esv3817314

Organism: Homo sapiens

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

Variant Calls:71
Validation:Not tested
Clinical Assertions: No
Region Size:3,397

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: 455 SVs from 36 studies. See in: genome view

Remapped(Score: Perfect):125,856,777-125,862,173

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3817314	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
esv3817314	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000023.10	ChrX	124,991,759 (-1000, +500)	124,995,155 (-500, +1000)

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
essv16850093	deletion	SAMN00009088	Sequencing	Read depth and paired-end mapping	Heterozygous	2,888
essv16850094	deletion	SAMN00016974	Sequencing	Read depth and paired-end mapping	Heterozygous	2,666
essv16850095	deletion	SAMN00016978	Sequencing	Read depth and paired-end mapping	Heterozygous	2,554
essv16850096	deletion	SAMN00016980	Sequencing	Read depth and paired-end mapping	Heterozygous	2,748
essv16850097	deletion	SAMN00006353	Sequencing	Read depth and paired-end mapping	Heterozygous	2,837
essv16850098	deletion	SAMN00009091	Sequencing	Read depth and paired-end mapping	Heterozygous	2,832
essv16850099	deletion	SAMN00006369	Sequencing	Read depth and paired-end mapping	Heterozygous	2,742
essv16850100	deletion	SAMN00006388	Sequencing	Read depth and paired-end mapping	Heterozygous	2,552
essv16850101	deletion	SAMN00006396	Sequencing	Read depth and paired-end mapping	Heterozygous	2,475
essv16850102	deletion	SAMN00006413	Sequencing	Read depth and paired-end mapping	Heterozygous	2,645
essv16850103	deletion	SAMN00006414	Sequencing	Read depth and paired-end mapping	Heterozygous	2,676
essv16850104	deletion	SAMN00006416	Sequencing	Read depth and paired-end mapping	Heterozygous	2,728
essv16850105	deletion	SAMN00006419	Sequencing	Read depth and paired-end mapping	Heterozygous	2,762
essv16850106	deletion	SAMN00006483	Sequencing	Read depth and paired-end mapping	Heterozygous	2,754
essv16850107	deletion	SAMN00006513	Sequencing	Read depth and paired-end mapping	Heterozygous	2,688
essv16850108	deletion	SAMN00006534	Sequencing	Read depth and paired-end mapping	Heterozygous	2,800
essv16850109	deletion	SAMN00009247	Sequencing	Read depth and paired-end mapping	Heterozygous	2,707
essv16850110	deletion	SAMN00014359	Sequencing	Read depth and paired-end mapping	Heterozygous	2,859
essv16850111	deletion	SAMN00014371	Sequencing	Read depth and paired-end mapping	Heterozygous	2,977
essv16850112	deletion	SAMN00249675	Sequencing	Read depth and paired-end mapping	Heterozygous	2,908
essv16850113	deletion	SAMN00249678	Sequencing	Read depth and paired-end mapping	Heterozygous	2,981
essv16850114	deletion	SAMN00249812	Sequencing	Read depth and paired-end mapping	Heterozygous	2,868
essv16850115	deletion	SAMN00014418	Sequencing	Read depth and paired-end mapping	Heterozygous	2,699
essv16850116	deletion	SAMN00016833	Sequencing	Read depth and paired-end mapping	Heterozygous	3,002
essv16850117	deletion	SAMN00016836	Sequencing	Read depth and paired-end mapping	Heterozygous	2,821
essv16850118	deletion	SAMN00016859	Sequencing	Read depth and paired-end mapping	Heterozygous	2,569
essv16850119	deletion	SAMN00249841	Sequencing	Read depth and paired-end mapping	Heterozygous	2,709
essv16850120	deletion	SAMN00249711	Sequencing	Read depth and paired-end mapping	Heterozygous	2,674
essv16850121	deletion	SAMN00263022	Sequencing	Read depth and paired-end mapping	Heterozygous	2,826
essv16850122	deletion	SAMN01091143	Sequencing	Read depth and paired-end mapping	Heterozygous	2,460
essv16850123	deletion	SAMN00255156	Sequencing	Read depth and paired-end mapping	Heterozygous	2,795
essv16850124	deletion	SAMN01761208	Sequencing	Read depth and paired-end mapping	Heterozygous	3,316
essv16850125	deletion	SAMN01036766	Sequencing	Read depth and paired-end mapping	Heterozygous	2,929
essv16850126	deletion	SAMN01036739	Sequencing	Read depth and paired-end mapping	Heterozygous	2,952
essv16850127	deletion	SAMN01096691	Sequencing	Read depth and paired-end mapping	Heterozygous	2,652
essv16850128	deletion	SAMN01761348	Sequencing	Read depth and paired-end mapping	Heterozygous	3,263
essv16850129	deletion	SAMN01090816	Sequencing	Read depth and paired-end mapping	Heterozygous	3,025
essv16850130	deletion	SAMN01096710	Sequencing	Read depth and paired-end mapping	Heterozygous	2,613
essv16850131	deletion	SAMN01761414	Sequencing	Read depth and paired-end mapping	Heterozygous	2,367
essv16850132	deletion	SAMN01096685	Sequencing	Read depth and paired-end mapping	Heterozygous	2,673
essv16850133	deletion	SAMN01090957	Sequencing	Read depth and paired-end mapping	Heterozygous	2,594
essv16850134	deletion	SAMN01761446	Sequencing	Read depth and paired-end mapping	Heterozygous	2,494
essv16850135	deletion	SAMN00001530	Sequencing	Read depth and paired-end mapping	Heterozygous	2,784
essv16850136	deletion	SAMN00801878	Sequencing	Read depth and paired-end mapping	Heterozygous	2,500
essv16850137	deletion	SAMN00004417	Sequencing	Read depth and paired-end mapping	Heterozygous	2,955
essv16850138	deletion	SAMN00001590	Sequencing	Read depth and paired-end mapping	Heterozygous	3,076
essv16850139	deletion	SAMN00000941	Sequencing	Read depth and paired-end mapping	Heterozygous	2,287
essv16850140	deletion	SAMN00001623	Sequencing	Read depth and paired-end mapping	Heterozygous	3,153
essv16850141	deletion	SAMN00001045	Sequencing	Read depth and paired-end mapping	Heterozygous	3,184
essv16850142	deletion	SAMN00000539	Sequencing	Read depth and paired-end mapping	Heterozygous	2,789
essv16850143	deletion	SAMN00001675	Sequencing	Read depth and paired-end mapping	Heterozygous	2,942
essv16850144	deletion	SAMN00000567	Sequencing	Read depth and paired-end mapping	Heterozygous	2,537
essv16850145	deletion	SAMN00001102	Sequencing	Read depth and paired-end mapping	Heterozygous	2,846
essv16850146	deletion	SAMN00001123	Sequencing	Read depth and paired-end mapping	Heterozygous	3,160
essv16850147	deletion	SAMN00001129	Sequencing	Read depth and paired-end mapping	Heterozygous	3,123
essv16850148	deletion	SAMN00001132	Sequencing	Read depth and paired-end mapping	Heterozygous	2,992
essv16850149	deletion	SAMN00001140	Sequencing	Read depth and paired-end mapping	Heterozygous	3,101
essv16850150	deletion	SAMN00001181	Sequencing	Read depth and paired-end mapping	Heterozygous	2,491
essv16850151	deletion	SAMN00001191	Sequencing	Read depth and paired-end mapping	Heterozygous	2,982
essv16850152	deletion	SAMN00007764	Sequencing	Read depth and paired-end mapping	Heterozygous	2,094
essv16850153	deletion	SAMN00007873	Sequencing	Read depth and paired-end mapping	Heterozygous	2,690
essv16850154	deletion	SAMN00001226	Sequencing	Read depth and paired-end mapping	Heterozygous	3,613
essv16850155	deletion	SAMN00001235	Sequencing	Read depth and paired-end mapping	Heterozygous	2,831
essv16850156	deletion	SAMN00001249	Sequencing	Read depth and paired-end mapping	Heterozygous	3,557
essv16850157	deletion	SAMN00001252	Sequencing	Read depth and paired-end mapping	Heterozygous	3,317
essv16850158	deletion	SAMN00001258	Sequencing	Read depth and paired-end mapping	Heterozygous	2,841
essv16850159	deletion	SAMN00001290	Sequencing	Read depth and paired-end mapping	Heterozygous	2,785
essv16850160	deletion	SAMN00001297	Sequencing	Read depth and paired-end mapping	Heterozygous	2,857
essv16850161	deletion	SAMN00001303	Sequencing	Read depth and paired-end mapping	Heterozygous	2,621
essv16850162	deletion	SAMN00001305	Sequencing	Read depth and paired-end mapping	Heterozygous	2,589
essv16850163	deletion	SAMN00007968	Sequencing	Read depth and paired-end mapping	Heterozygous	2,736

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv16850093	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850094	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850095	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850096	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850097	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850098	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850099	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850100	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850101	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850102	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850103	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850104	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850105	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850106	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850107	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850108	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850109	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850110	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850111	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850112	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850113	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850114	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850115	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850116	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850117	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850118	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850119	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850120	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850121	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850122	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850123	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850124	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850125	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850126	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850127	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850128	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850129	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850130	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850131	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850132	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850133	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850134	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850135	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850136	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850137	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850138	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850139	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850140	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850141	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850142	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850143	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850144	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850145	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850146	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850147	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850148	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850149	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850150	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850151	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850152	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850153	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850154	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850155	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850156	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850157	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850158	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850159	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850160	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850161	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850162	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850163	Remapped	Perfect	NC_000023.11:g.(12 5856777_125858277) _(125860673_125862 173)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	125,857,777 (-1000, +500)	125,861,173 (-500, +1000)
essv16850093	Submitted genomic		NC_000023.10:g.(12 4990759_124992259) _(124994655_124996 155)del	GRCh37 (hg19)		NC_000023.10	ChrX	124,991,759 (-1000, +500)	124,995,155 (-500, +1000)
essv16850094	Submitted genomic		NC_000023.10:g.(12 4990759_124992259) _(124994655_124996 155)del	GRCh37 (hg19)		NC_000023.10	ChrX	124,991,759 (-1000, +500)	124,995,155 (-500, +1000)
essv16850095	Submitted genomic		NC_000023.10:g.(12 4990759_124992259) _(124994655_124996 155)del	GRCh37 (hg19)		NC_000023.10	ChrX	124,991,759 (-1000, +500)	124,995,155 (-500, +1000)
essv16850096	Submitted genomic		NC_000023.10:g.(12 4990759_124992259) _(124994655_124996 155)del	GRCh37 (hg19)		NC_000023.10	ChrX	124,991,759 (-1000, +500)	124,995,155 (-500, +1000)
essv16850097	Submitted genomic		NC_000023.10:g.(12 4990759_124992259) _(124994655_124996 155)del	GRCh37 (hg19)		NC_000023.10	ChrX	124,991,759 (-1000, +500)	124,995,155 (-500, +1000)
essv16850098	Submitted genomic		NC_000023.10:g.(12 4990759_124992259) _(124994655_124996 155)del	GRCh37 (hg19)		NC_000023.10	ChrX	124,991,759 (-1000, +500)	124,995,155 (-500, +1000)
essv16850099	Submitted genomic		NC_000023.10:g.(12 4990759_124992259) _(124994655_124996 155)del	GRCh37 (hg19)		NC_000023.10	ChrX	124,991,759 (-1000, +500)	124,995,155 (-500, +1000)
essv16850100	Submitted genomic		NC_000023.10:g.(12 4990759_124992259) _(124994655_124996 155)del	GRCh37 (hg19)		NC_000023.10	ChrX	124,991,759 (-1000, +500)	124,995,155 (-500, +1000)
essv16850101	Submitted genomic		NC_000023.10:g.(12 4990759_124992259) _(124994655_124996 155)del	GRCh37 (hg19)		NC_000023.10	ChrX	124,991,759 (-1000, +500)	124,995,155 (-500, +1000)
essv16850102	Submitted genomic		NC_000023.10:g.(12 4990759_124992259) _(124994655_124996 155)del	GRCh37 (hg19)		NC_000023.10	ChrX	124,991,759 (-1000, +500)	124,995,155 (-500, +1000)
essv16850103	Submitted genomic		NC_000023.10:g.(12 4990759_124992259) _(124994655_124996 155)del	GRCh37 (hg19)		NC_000023.10	ChrX	124,991,759 (-1000, +500)	124,995,155 (-500, +1000)
essv16850104	Submitted genomic		NC_000023.10:g.(12 4990759_124992259) _(124994655_124996 155)del	GRCh37 (hg19)		NC_000023.10	ChrX	124,991,759 (-1000, +500)	124,995,155 (-500, +1000)
essv16850105	Submitted genomic		NC_000023.10:g.(12 4990759_124992259) _(124994655_124996 155)del	GRCh37 (hg19)		NC_000023.10	ChrX	124,991,759 (-1000, +500)	124,995,155 (-500, +1000)
essv16850106	Submitted genomic		NC_000023.10:g.(12 4990759_124992259) _(124994655_124996 155)del	GRCh37 (hg19)		NC_000023.10	ChrX	124,991,759 (-1000, +500)	124,995,155 (-500, +1000)
essv16850107	Submitted genomic		NC_000023.10:g.(12 4990759_124992259) _(124994655_124996 155)del	GRCh37 (hg19)		NC_000023.10	ChrX	124,991,759 (-1000, +500)	124,995,155 (-500, +1000)
essv16850108	Submitted genomic		NC_000023.10:g.(12 4990759_124992259) _(124994655_124996 155)del	GRCh37 (hg19)		NC_000023.10	ChrX	124,991,759 (-1000, +500)	124,995,155 (-500, +1000)
essv16850109	Submitted genomic		NC_000023.10:g.(12 4990759_124992259) _(124994655_124996 155)del	GRCh37 (hg19)		NC_000023.10	ChrX	124,991,759 (-1000, +500)	124,995,155 (-500, +1000)
essv16850110	Submitted genomic		NC_000023.10:g.(12 4990759_124992259) _(124994655_124996 155)del	GRCh37 (hg19)		NC_000023.10	ChrX	124,991,759 (-1000, +500)	124,995,155 (-500, +1000)
essv16850111	Submitted genomic		NC_000023.10:g.(12 4990759_124992259) _(124994655_124996 155)del	GRCh37 (hg19)		NC_000023.10	ChrX	124,991,759 (-1000, +500)	124,995,155 (-500, +1000)
essv16850112	Submitted genomic		NC_000023.10:g.(12 4990759_124992259) _(124994655_124996 155)del	GRCh37 (hg19)		NC_000023.10	ChrX	124,991,759 (-1000, +500)	124,995,155 (-500, +1000)
essv16850113	Submitted genomic		NC_000023.10:g.(12 4990759_124992259) _(124994655_124996 155)del	GRCh37 (hg19)		NC_000023.10	ChrX	124,991,759 (-1000, +500)	124,995,155 (-500, +1000)
essv16850114	Submitted genomic		NC_000023.10:g.(12 4990759_124992259) _(124994655_124996 155)del	GRCh37 (hg19)		NC_000023.10	ChrX	124,991,759 (-1000, +500)	124,995,155 (-500, +1000)
essv16850115	Submitted genomic		NC_000023.10:g.(12 4990759_124992259) _(124994655_124996 155)del	GRCh37 (hg19)		NC_000023.10	ChrX	124,991,759 (-1000, +500)	124,995,155 (-500, +1000)
essv16850116	Submitted genomic		NC_000023.10:g.(12 4990759_124992259) _(124994655_124996 155)del	GRCh37 (hg19)		NC_000023.10	ChrX	124,991,759 (-1000, +500)	124,995,155 (-500, +1000)
essv16850117	Submitted genomic		NC_000023.10:g.(12 4990759_124992259) _(124994655_124996 155)del	GRCh37 (hg19)		NC_000023.10	ChrX	124,991,759 (-1000, +500)	124,995,155 (-500, +1000)
essv16850118	Submitted genomic		NC_000023.10:g.(12 4990759_124992259) _(124994655_124996 155)del	GRCh37 (hg19)		NC_000023.10	ChrX	124,991,759 (-1000, +500)	124,995,155 (-500, +1000)
essv16850119	Submitted genomic		NC_000023.10:g.(12 4990759_124992259) _(124994655_124996 155)del	GRCh37 (hg19)		NC_000023.10	ChrX	124,991,759 (-1000, +500)	124,995,155 (-500, +1000)
essv16850120	Submitted genomic		NC_000023.10:g.(12 4990759_124992259) _(124994655_124996 155)del	GRCh37 (hg19)		NC_000023.10	ChrX	124,991,759 (-1000, +500)	124,995,155 (-500, +1000)
essv16850121	Submitted genomic		NC_000023.10:g.(12 4990759_124992259) _(124994655_124996 155)del	GRCh37 (hg19)		NC_000023.10	ChrX	124,991,759 (-1000, +500)	124,995,155 (-500, +1000)

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dbVar

Database of genomic structural variation

esv3817314

Links to Other Resources

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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.