esv3817420

Organism: Homo sapiens

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

Variant Calls:904
Validation:Not tested
Clinical Assertions: No
Region Size:14,941

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: 632 SVs from 51 studies. See in: genome view

Submitted genomic115,137,622-115,153,304

Variant Region Placement Information

Variant Region ID	Placement Type	Assembly	Assembly Unit	Sequence ID	Chr	Start	Stop
esv3817420	Submitted genomic	GRCh37 (hg19)	Primary Assembly	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
essv16864000	deletion	SAMN00004626	Sequencing	Read depth and paired-end mapping	Homozygous	2,931
essv16864001	deletion	SAMN00004627	Sequencing	Read depth and paired-end mapping	Heterozygous	2,692
essv16864002	deletion	SAMN00004628	Sequencing	Read depth and paired-end mapping	Heterozygous	2,684
essv16864003	deletion	SAMN00004636	Sequencing	Read depth and paired-end mapping	Heterozygous	2,698
essv16864004	deletion	SAMN00004637	Sequencing	Read depth and paired-end mapping	Heterozygous	2,609
essv16864005	deletion	SAMN00004639	Sequencing	Read depth and paired-end mapping	Heterozygous	2,703
essv16864006	deletion	SAMN00004640	Sequencing	Read depth and paired-end mapping	Heterozygous	2,393
essv16864007	deletion	SAMN00004641	Sequencing	Read depth and paired-end mapping	Heterozygous	2,942
essv16864008	deletion	SAMN00006337	Sequencing	Read depth and paired-end mapping	Homozygous	2,882
essv16864009	deletion	SAMN00004644	Sequencing	Read depth and paired-end mapping	Heterozygous	2,699
essv16864010	deletion	SAMN00006340	Sequencing	Read depth and paired-end mapping	Heterozygous	2,731
essv16864011	deletion	SAMN00006341	Sequencing	Read depth and paired-end mapping	Heterozygous	2,683
essv16864012	deletion	SAMN00006343	Sequencing	Read depth and paired-end mapping	Heterozygous	2,433
essv16864013	deletion	SAMN00004646	Sequencing	Read depth and paired-end mapping	Heterozygous	2,568
essv16864014	deletion	SAMN00004647	Sequencing	Read depth and paired-end mapping	Heterozygous	2,660
essv16864015	deletion	SAMN00004648	Sequencing	Read depth and paired-end mapping	Heterozygous	2,529
essv16864016	deletion	SAMN00004649	Sequencing	Read depth and paired-end mapping	Heterozygous	2,793
essv16864017	deletion	SAMN00004658	Sequencing	Read depth and paired-end mapping	Heterozygous	2,650
essv16864018	deletion	SAMN00004660	Sequencing	Read depth and paired-end mapping	Heterozygous	2,465
essv16864019	deletion	SAMN00009088	Sequencing	Read depth and paired-end mapping	Homozygous	2,888
essv16864020	deletion	SAMN00004675	Sequencing	Read depth and paired-end mapping	Heterozygous	2,600
essv16864021	deletion	SAMN00004676	Sequencing	Read depth and paired-end mapping	Heterozygous	2,580
essv16864022	deletion	SAMN00016965	Sequencing	Read depth and paired-end mapping	Homozygous	2,566
essv16864023	deletion	SAMN00016966	Sequencing	Read depth and paired-end mapping	Heterozygous	2,448
essv16864024	deletion	SAMN00016968	Sequencing	Read depth and paired-end mapping	Heterozygous	2,820
essv16864025	deletion	SAMN00016969	Sequencing	Read depth and paired-end mapping	Heterozygous	2,443
essv16864026	deletion	SAMN00016971	Sequencing	Read depth and paired-end mapping	Heterozygous	2,465
essv16864027	deletion	SAMN00016974	Sequencing	Read depth and paired-end mapping	Heterozygous	2,666
essv16864028	deletion	SAMN00016975	Sequencing	Read depth and paired-end mapping	Heterozygous	2,531
essv16864029	deletion	SAMN00016977	Sequencing	Read depth and paired-end mapping	Heterozygous	2,562
essv16864030	deletion	SAMN00006346	Sequencing	Read depth and paired-end mapping	Heterozygous	2,602
essv16864031	deletion	SAMN00006347	Sequencing	Read depth and paired-end mapping	Homozygous	2,456
essv16864032	deletion	SAMN00004678	Sequencing	Read depth and paired-end mapping	Heterozygous	2,465
essv16864033	deletion	SAMN00004679	Sequencing	Read depth and paired-end mapping	Heterozygous	2,446
essv16864034	deletion	SAMN00006348	Sequencing	Read depth and paired-end mapping	Heterozygous	2,664
essv16864035	deletion	SAMN00006349	Sequencing	Read depth and paired-end mapping	Heterozygous	2,741
essv16864036	deletion	SAMN00004680	Sequencing	Read depth and paired-end mapping	Homozygous	2,630
essv16864037	deletion	SAMN00006350	Sequencing	Read depth and paired-end mapping	Homozygous	2,652
essv16864038	deletion	SAMN00004681	Sequencing	Read depth and paired-end mapping	Heterozygous	2,727
essv16864039	deletion	SAMN00006351	Sequencing	Read depth and paired-end mapping	Heterozygous	2,773
essv16864040	deletion	SAMN00006353	Sequencing	Read depth and paired-end mapping	Heterozygous	2,837
essv16864041	deletion	SAMN00006354	Sequencing	Read depth and paired-end mapping	Homozygous	2,703
essv16864042	deletion	SAMN00009089	Sequencing	Read depth and paired-end mapping	Heterozygous	2,585
essv16864043	deletion	SAMN00009091	Sequencing	Read depth and paired-end mapping	Heterozygous	2,832
essv16864044	deletion	SAMN00009092	Sequencing	Read depth and paired-end mapping	Heterozygous	2,808
essv16864045	deletion	SAMN00006358	Sequencing	Read depth and paired-end mapping	Heterozygous	2,757
essv16864046	deletion	SAMN00006359	Sequencing	Read depth and paired-end mapping	Heterozygous	2,753
essv16864047	deletion	SAMN00006362	Sequencing	Read depth and paired-end mapping	Heterozygous	2,917
essv16864048	deletion	SAMN00006365	Sequencing	Read depth and paired-end mapping	Homozygous	2,690
essv16864049	deletion	SAMN00006366	Sequencing	Read depth and paired-end mapping	Homozygous	2,730
essv16864050	deletion	SAMN00006370	Sequencing	Read depth and paired-end mapping	Homozygous	2,238
essv16864051	deletion	SAMN00006372	Sequencing	Read depth and paired-end mapping	Homozygous	2,697
essv16864052	deletion	SAMN00006373	Sequencing	Read depth and paired-end mapping	Heterozygous	2,538
essv16864053	deletion	SAMN00006375	Sequencing	Read depth and paired-end mapping	Heterozygous	2,780
essv16864054	deletion	SAMN00006376	Sequencing	Read depth and paired-end mapping	Heterozygous	2,448
essv16864055	deletion	SAMN00006377	Sequencing	Read depth and paired-end mapping	Heterozygous	2,795
essv16864056	deletion	SAMN00009093	Sequencing	Read depth and paired-end mapping	Heterozygous	2,361
essv16864057	deletion	SAMN00009094	Sequencing	Read depth and paired-end mapping	Homozygous	2,610
essv16864058	deletion	SAMN00009097	Sequencing	Read depth and paired-end mapping	Heterozygous	2,768
essv16864059	deletion	SAMN00009098	Sequencing	Read depth and paired-end mapping	Heterozygous	2,704
essv16864060	deletion	SAMN00009099	Sequencing	Read depth and paired-end mapping	Heterozygous	2,678
essv16864061	deletion	SAMN01761612	Sequencing	Read depth and paired-end mapping	Heterozygous	2,789
essv16864062	deletion	SAMN01761624	Sequencing	Read depth and paired-end mapping	Heterozygous	2,255
essv16864063	deletion	SAMN00006378	Sequencing	Read depth and paired-end mapping	Heterozygous	2,702
essv16864064	deletion	SAMN00006380	Sequencing	Read depth and paired-end mapping	Heterozygous	2,770
essv16864065	deletion	SAMN00006381	Sequencing	Read depth and paired-end mapping	Heterozygous	2,721
essv16864066	deletion	SAMN00006384	Sequencing	Read depth and paired-end mapping	Heterozygous	2,392
essv16864067	deletion	SAMN00006385	Sequencing	Read depth and paired-end mapping	Heterozygous	2,419
essv16864068	deletion	SAMN00006386	Sequencing	Read depth and paired-end mapping	Heterozygous	2,544
essv16864069	deletion	SAMN00006387	Sequencing	Read depth and paired-end mapping	Heterozygous	2,527
essv16864070	deletion	SAMN00006388	Sequencing	Read depth and paired-end mapping	Heterozygous	2,552
essv16864071	deletion	SAMN00009104	Sequencing	Read depth and paired-end mapping	Heterozygous	2,613
essv16864072	deletion	SAMN00009106	Sequencing	Read depth and paired-end mapping	Heterozygous	2,582
essv16864073	deletion	SAMN00006390	Sequencing	Read depth and paired-end mapping	Homozygous	2,374
essv16864074	deletion	SAMN00009111	Sequencing	Read depth and paired-end mapping	Heterozygous	2,696
essv16864075	deletion	SAMN00006394	Sequencing	Read depth and paired-end mapping	Heterozygous	2,847
essv16864076	deletion	SAMN00006396	Sequencing	Read depth and paired-end mapping	Heterozygous	2,475
essv16864077	deletion	SAMN00009112	Sequencing	Read depth and paired-end mapping	Heterozygous	2,788
essv16864078	deletion	SAMN00006397	Sequencing	Read depth and paired-end mapping	Heterozygous	2,768
essv16864079	deletion	SAMN00006399	Sequencing	Read depth and paired-end mapping	Homozygous	2,300
essv16864080	deletion	SAMN00006403	Sequencing	Read depth and paired-end mapping	Heterozygous	2,464
essv16864081	deletion	SAMN00006406	Sequencing	Read depth and paired-end mapping	Heterozygous	2,406
essv16864082	deletion	SAMN00006411	Sequencing	Read depth and paired-end mapping	Heterozygous	2,770
essv16864083	deletion	SAMN00006412	Sequencing	Read depth and paired-end mapping	Homozygous	3,016
essv16864084	deletion	SAMN00006413	Sequencing	Read depth and paired-end mapping	Heterozygous	2,645
essv16864085	deletion	SAMN00006414	Sequencing	Read depth and paired-end mapping	Homozygous	2,676
essv16864086	deletion	SAMN00006417	Sequencing	Read depth and paired-end mapping	Homozygous	2,428
essv16864087	deletion	SAMN00006418	Sequencing	Read depth and paired-end mapping	Heterozygous	2,864
essv16864088	deletion	SAMN00006420	Sequencing	Read depth and paired-end mapping	Heterozygous	2,805
essv16864089	deletion	SAMN00006421	Sequencing	Read depth and paired-end mapping	Heterozygous	2,532
essv16864090	deletion	SAMN00006422	Sequencing	Read depth and paired-end mapping	Heterozygous	2,348
essv16864091	deletion	SAMN00006423	Sequencing	Read depth and paired-end mapping	Heterozygous	2,729
essv16864092	deletion	SAMN00006424	Sequencing	Read depth and paired-end mapping	Heterozygous	2,745
essv16864093	deletion	SAMN00006428	Sequencing	Read depth and paired-end mapping	Heterozygous	2,754
essv16864094	deletion	SAMN00006429	Sequencing	Read depth and paired-end mapping	Heterozygous	2,737
essv16864095	deletion	SAMN00009113	Sequencing	Read depth and paired-end mapping	Heterozygous	2,679
essv16864096	deletion	SAMN00006431	Sequencing	Read depth and paired-end mapping	Heterozygous	2,696
essv16864097	deletion	SAMN00006435	Sequencing	Read depth and paired-end mapping	Heterozygous	2,697
essv16864098	deletion	SAMN00006436	Sequencing	Read depth and paired-end mapping	Heterozygous	2,677
essv16864099	deletion	SAMN00006448	Sequencing	Read depth and paired-end mapping	Heterozygous	2,923

Showing 100 of 904

Variant Call Placement Information

Variant Call ID	Placement Type	HGVS	Assembly	Sequence ID	Chr	Start	Stop
essv16864000	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864001	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864002	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864003	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864004	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864005	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864006	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864007	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864008	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864009	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864010	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864011	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864012	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864013	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864014	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864015	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864016	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864017	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864018	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864019	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864020	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864021	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864022	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864023	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864024	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864025	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864026	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864027	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864028	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864029	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864030	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864031	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864032	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864033	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864034	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864035	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864036	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864037	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864038	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864039	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864040	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864041	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864042	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864043	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864044	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864045	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864046	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864047	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864048	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864049	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864050	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864051	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864052	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864053	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864054	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864055	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864056	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864057	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864058	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864059	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864060	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864061	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864062	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864063	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864064	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864065	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864066	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864067	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864068	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864069	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864070	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864071	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864072	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864073	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864074	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864075	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864076	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864077	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864078	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864079	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864080	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864081	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864082	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864083	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864084	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864085	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864086	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864087	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864088	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864089	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864090	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864091	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864092	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864093	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864094	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864095	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864096	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864097	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864098	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)
essv16864099	Submitted genomic	NC_000023.10:g.(11 5137622_115137999) _(115152939_115153 304)del	GRCh37 (hg19)	NC_000023.10	ChrX	115,137,999 (-377, +0)	115,152,939 (-0, +365)

Showing 100 of 904

dbVar

Database of genomic structural variation

esv3817420

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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.