esv3587491

Organism: Homo sapiens

Study:estd214 (1000 Genomes Consortium Phase 3)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh37

Variant Calls:2,473
Validation:Not tested
Clinical Assertions: No
Region Size:40,659

Publication(s):1000 Genomes Project Consortium et al. 2015

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 375 SVs from 51 studies. See in: genome view

Remapped(Score: Good):120,868,540-120,910,198

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3587491	Remapped	Good	GRCh38.p12	Primary Assembly	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
esv3587491	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000001.10	Chr1	149,532,289 (-500, +0)	149,572,952 (-0, +500)

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
essv10137822	deletion	SAMN00004622	Sequencing	Read depth and paired-end mapping	Homozygous	2,214
essv10137823	deletion	SAMN00004623	Sequencing	Read depth and paired-end mapping	Homozygous	2,667
essv10137824	deletion	SAMN00004625	Sequencing	Read depth and paired-end mapping	Homozygous	2,591
essv10137825	deletion	SAMN00004626	Sequencing	Read depth and paired-end mapping	Homozygous	2,931
essv10137826	deletion	SAMN00004627	Sequencing	Read depth and paired-end mapping	Heterozygous	2,692
essv10137827	deletion	SAMN00004628	Sequencing	Read depth and paired-end mapping	Homozygous	2,684
essv10137828	deletion	SAMN00004629	Sequencing	Read depth and paired-end mapping	Homozygous	2,200
essv10137829	deletion	SAMN00004631	Sequencing	Read depth and paired-end mapping	Homozygous	2,737
essv10137830	deletion	SAMN00004632	Sequencing	Read depth and paired-end mapping	Homozygous	2,666
essv10137831	deletion	SAMN00004633	Sequencing	Read depth and paired-end mapping	Homozygous	2,664
essv10137832	deletion	SAMN00004634	Sequencing	Read depth and paired-end mapping	Homozygous	2,737
essv10137833	deletion	SAMN00004635	Sequencing	Read depth and paired-end mapping	Homozygous	2,821
essv10137834	deletion	SAMN00004636	Sequencing	Read depth and paired-end mapping	Homozygous	2,698
essv10137835	deletion	SAMN00004637	Sequencing	Read depth and paired-end mapping	Homozygous	2,609
essv10137836	deletion	SAMN00004638	Sequencing	Read depth and paired-end mapping	Homozygous	2,504
essv10137837	deletion	SAMN00004639	Sequencing	Read depth and paired-end mapping	Homozygous	2,703
essv10137838	deletion	SAMN00004640	Sequencing	Read depth and paired-end mapping	Homozygous	2,393
essv10137839	deletion	SAMN00004641	Sequencing	Read depth and paired-end mapping	Homozygous	2,942
essv10137840	deletion	SAMN00004642	Sequencing	Read depth and paired-end mapping	Homozygous	2,702
essv10137841	deletion	SAMN00004643	Sequencing	Read depth and paired-end mapping	Homozygous	2,552
essv10137842	deletion	SAMN00006337	Sequencing	Read depth and paired-end mapping	Homozygous	2,882
essv10137843	deletion	SAMN00006338	Sequencing	Read depth and paired-end mapping	Homozygous	2,748
essv10137844	deletion	SAMN00004644	Sequencing	Read depth and paired-end mapping	Homozygous	2,699
essv10137845	deletion	SAMN00006339	Sequencing	Read depth and paired-end mapping	Homozygous	2,741
essv10137846	deletion	SAMN00006340	Sequencing	Read depth and paired-end mapping	Homozygous	2,731
essv10137847	deletion	SAMN00006341	Sequencing	Read depth and paired-end mapping	Homozygous	2,683
essv10137848	deletion	SAMN00006343	Sequencing	Read depth and paired-end mapping	Homozygous	2,433
essv10137849	deletion	SAMN00006344	Sequencing	Read depth and paired-end mapping	Homozygous	2,768
essv10137850	deletion	SAMN00004645	Sequencing	Read depth and paired-end mapping	Homozygous	2,148
essv10137851	deletion	SAMN00004646	Sequencing	Read depth and paired-end mapping	Homozygous	2,568
essv10137852	deletion	SAMN00004647	Sequencing	Read depth and paired-end mapping	Homozygous	2,660
essv10137853	deletion	SAMN00004648	Sequencing	Read depth and paired-end mapping	Homozygous	2,529
essv10137854	deletion	SAMN00004649	Sequencing	Read depth and paired-end mapping	Homozygous	2,793
essv10137855	deletion	SAMN00004650	Sequencing	Read depth and paired-end mapping	Homozygous	2,682
essv10137856	deletion	SAMN00004651	Sequencing	Read depth and paired-end mapping	Homozygous	2,831
essv10137857	deletion	SAMN00004654	Sequencing	Read depth and paired-end mapping	Homozygous	2,593
essv10137858	deletion	SAMN00004655	Sequencing	Read depth and paired-end mapping	Homozygous	2,454
essv10137859	deletion	SAMN00004656	Sequencing	Read depth and paired-end mapping	Homozygous	2,595
essv10137860	deletion	SAMN00004657	Sequencing	Read depth and paired-end mapping	Homozygous	2,763
essv10137861	deletion	SAMN00004658	Sequencing	Read depth and paired-end mapping	Homozygous	2,650
essv10137862	deletion	SAMN00004659	Sequencing	Read depth and paired-end mapping	Homozygous	2,876
essv10137863	deletion	SAMN00004660	Sequencing	Read depth and paired-end mapping	Homozygous	2,465
essv10137864	deletion	SAMN00004661	Sequencing	Read depth and paired-end mapping	Homozygous	2,731
essv10137865	deletion	SAMN00004663	Sequencing	Read depth and paired-end mapping	Homozygous	2,670
essv10137866	deletion	SAMN00004664	Sequencing	Read depth and paired-end mapping	Homozygous	2,739
essv10137867	deletion	SAMN00004666	Sequencing	Read depth and paired-end mapping	Homozygous	2,758
essv10137868	deletion	SAMN00004667	Sequencing	Read depth and paired-end mapping	Homozygous	2,709
essv10137869	deletion	SAMN00004668	Sequencing	Read depth and paired-end mapping	Homozygous	2,231
essv10137870	deletion	SAMN00004669	Sequencing	Read depth and paired-end mapping	Homozygous	2,753
essv10137871	deletion	SAMN00009088	Sequencing	Read depth and paired-end mapping	Homozygous	2,888
essv10137872	deletion	SAMN00004672	Sequencing	Read depth and paired-end mapping	Homozygous	2,782
essv10137873	deletion	SAMN00004674	Sequencing	Read depth and paired-end mapping	Homozygous	2,809
essv10137874	deletion	SAMN00004675	Sequencing	Read depth and paired-end mapping	Homozygous	2,600
essv10137875	deletion	SAMN00006345	Sequencing	Read depth and paired-end mapping	Homozygous	2,777
essv10137876	deletion	SAMN00004676	Sequencing	Read depth and paired-end mapping	Homozygous	2,580
essv10137877	deletion	SAMN00016965	Sequencing	Read depth and paired-end mapping	Homozygous	2,566
essv10137878	deletion	SAMN00016966	Sequencing	Read depth and paired-end mapping	Homozygous	2,448
essv10137879	deletion	SAMN00016967	Sequencing	Read depth and paired-end mapping	Homozygous	2,522
essv10137880	deletion	SAMN00016968	Sequencing	Read depth and paired-end mapping	Homozygous	2,820
essv10137881	deletion	SAMN00016969	Sequencing	Read depth and paired-end mapping	Homozygous	2,443
essv10137882	deletion	SAMN00016970	Sequencing	Read depth and paired-end mapping	Homozygous	2,824
essv10137883	deletion	SAMN00016971	Sequencing	Read depth and paired-end mapping	Homozygous	2,465
essv10137884	deletion	SAMN00016972	Sequencing	Read depth and paired-end mapping	Homozygous	2,408
essv10137885	deletion	SAMN00016973	Sequencing	Read depth and paired-end mapping	Homozygous	2,813
essv10137886	deletion	SAMN00016974	Sequencing	Read depth and paired-end mapping	Homozygous	2,666
essv10137887	deletion	SAMN00016975	Sequencing	Read depth and paired-end mapping	Homozygous	2,531
essv10137888	deletion	SAMN00016976	Sequencing	Read depth and paired-end mapping	Homozygous	2,756
essv10137889	deletion	SAMN00016977	Sequencing	Read depth and paired-end mapping	Homozygous	2,562
essv10137890	deletion	SAMN00016978	Sequencing	Read depth and paired-end mapping	Homozygous	2,554
essv10137891	deletion	SAMN00016979	Sequencing	Read depth and paired-end mapping	Homozygous	2,879
essv10137892	deletion	SAMN00016980	Sequencing	Read depth and paired-end mapping	Homozygous	2,748
essv10137893	deletion	SAMN00016981	Sequencing	Read depth and paired-end mapping	Homozygous	2,774
essv10137894	deletion	SAMN00006346	Sequencing	Read depth and paired-end mapping	Homozygous	2,602
essv10137895	deletion	SAMN00006347	Sequencing	Read depth and paired-end mapping	Homozygous	2,456
essv10137896	deletion	SAMN00004677	Sequencing	Read depth and paired-end mapping	Homozygous	2,238
essv10137897	deletion	SAMN00004678	Sequencing	Read depth and paired-end mapping	Homozygous	2,465
essv10137898	deletion	SAMN00004679	Sequencing	Read depth and paired-end mapping	Homozygous	2,446
essv10137899	deletion	SAMN00006348	Sequencing	Read depth and paired-end mapping	Homozygous	2,664
essv10137900	deletion	SAMN00006349	Sequencing	Read depth and paired-end mapping	Homozygous	2,741
essv10137901	deletion	SAMN00004680	Sequencing	Read depth and paired-end mapping	Homozygous	2,630
essv10137902	deletion	SAMN00006350	Sequencing	Read depth and paired-end mapping	Homozygous	2,652
essv10137903	deletion	SAMN00004681	Sequencing	Read depth and paired-end mapping	Homozygous	2,727
essv10137904	deletion	SAMN00006351	Sequencing	Read depth and paired-end mapping	Homozygous	2,773
essv10137905	deletion	SAMN00006352	Sequencing	Read depth and paired-end mapping	Homozygous	2,799
essv10137906	deletion	SAMN00006353	Sequencing	Read depth and paired-end mapping	Homozygous	2,837
essv10137907	deletion	SAMN00006354	Sequencing	Read depth and paired-end mapping	Homozygous	2,703
essv10137908	deletion	SAMN00009089	Sequencing	Read depth and paired-end mapping	Homozygous	2,585
essv10137909	deletion	SAMN00009091	Sequencing	Read depth and paired-end mapping	Homozygous	2,832
essv10137910	deletion	SAMN00009092	Sequencing	Read depth and paired-end mapping	Homozygous	2,808
essv10137911	deletion	SAMN00006357	Sequencing	Read depth and paired-end mapping	Homozygous	2,740
essv10137912	deletion	SAMN00006358	Sequencing	Read depth and paired-end mapping	Homozygous	2,757
essv10137913	deletion	SAMN00006359	Sequencing	Read depth and paired-end mapping	Homozygous	2,753
essv10137914	deletion	SAMN00004682	Sequencing	Read depth and paired-end mapping	Homozygous	2,758
essv10137915	deletion	SAMN00006360	Sequencing	Read depth and paired-end mapping	Homozygous	2,737
essv10137916	deletion	SAMN00006361	Sequencing	Read depth and paired-end mapping	Homozygous	2,773
essv10137917	deletion	SAMN00006362	Sequencing	Read depth and paired-end mapping	Homozygous	2,917
essv10137918	deletion	SAMN00006363	Sequencing	Read depth and paired-end mapping	Homozygous	2,862
essv10137919	deletion	SAMN00006364	Sequencing	Read depth and paired-end mapping	Homozygous	2,776
essv10137920	deletion	SAMN00006365	Sequencing	Read depth and paired-end mapping	Homozygous	2,690
essv10137921	deletion	SAMN00006366	Sequencing	Read depth and paired-end mapping	Homozygous	2,730

Showing 100 of 2473

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv10137822	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137823	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137824	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137825	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137826	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137827	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137828	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137829	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137830	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137831	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137832	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137833	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137834	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137835	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137836	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137837	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137838	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137839	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137840	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137841	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137842	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137843	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137844	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137845	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137846	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137847	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137848	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137849	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137850	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137851	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137852	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137853	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137854	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137855	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137856	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137857	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137858	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137859	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137860	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137861	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137862	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137863	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137864	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137865	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137866	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137867	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137868	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137869	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137870	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137871	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137872	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137873	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137874	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137875	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137876	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137877	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137878	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137879	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137880	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137881	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137882	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137883	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137884	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137885	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137886	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137887	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137888	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137889	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137890	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137891	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137892	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137893	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137894	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137895	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137896	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137897	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137898	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137899	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137900	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137901	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137902	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137903	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137904	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137905	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137906	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137907	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137908	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137909	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137910	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137911	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137912	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137913	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137914	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137915	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137916	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137917	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137918	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137919	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137920	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)
essv10137921	Remapped	Good	NC_000001.11:g.(12 0868540_120869040) _(120909698_120910 198)del	GRCh38.p12	Second Pass	NC_000001.11	Chr1	120,869,040 (-500, +0)	120,909,698 (-0, +500)

Showing 100 of 4946

dbVar

Database of genomic structural variation

esv3587491

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Variant Region Placement Information

Variant Call Information

Variant Call Placement Information

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.