esv3817503

Organism: Homo sapiens

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

Variant Calls:188
Validation:Not tested
Clinical Assertions: No
Region Size:2,732

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: 871 SVs from 35 studies. See in: genome view

Remapped(Score: Perfect):782,589-786,026

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3817503	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
esv3817503	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000023.10	ChrX	743,673 (-349, +0)	746,404 (-0, +357)

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
essv16877838	deletion	SAMN00004632	Sequencing	Read depth and paired-end mapping	Heterozygous	2,666
essv16877839	deletion	SAMN00004633	Sequencing	Read depth and paired-end mapping	Heterozygous	2,664
essv16877840	deletion	SAMN00004637	Sequencing	Read depth and paired-end mapping	Heterozygous	2,609
essv16877841	deletion	SAMN00006340	Sequencing	Read depth and paired-end mapping	Heterozygous	2,731
essv16877842	deletion	SAMN00004648	Sequencing	Read depth and paired-end mapping	Heterozygous	2,529
essv16877843	deletion	SAMN00004661	Sequencing	Read depth and paired-end mapping	Heterozygous	2,731
essv16877844	deletion	SAMN00004675	Sequencing	Read depth and paired-end mapping	Heterozygous	2,600
essv16877845	deletion	SAMN00016971	Sequencing	Read depth and paired-end mapping	Heterozygous	2,465
essv16877846	deletion	SAMN00016976	Sequencing	Read depth and paired-end mapping	Homozygous	2,756
essv16877847	deletion	SAMN00006357	Sequencing	Read depth and paired-end mapping	Heterozygous	2,740
essv16877848	deletion	SAMN00006371	Sequencing	Read depth and paired-end mapping	Homozygous	2,644
essv16877849	deletion	SAMN00006376	Sequencing	Read depth and paired-end mapping	Heterozygous	2,448
essv16877850	deletion	SAMN00006377	Sequencing	Read depth and paired-end mapping	Heterozygous	2,795
essv16877851	deletion	SAMN00009093	Sequencing	Read depth and paired-end mapping	Heterozygous	2,361
essv16877852	deletion	SAMN00009094	Sequencing	Read depth and paired-end mapping	Heterozygous	2,610
essv16877853	deletion	SAMN00009096	Sequencing	Read depth and paired-end mapping	Heterozygous	2,592
essv16877854	deletion	SAMN00009098	Sequencing	Read depth and paired-end mapping	Heterozygous	2,704
essv16877855	deletion	SAMN00009100	Sequencing	Read depth and paired-end mapping	Heterozygous	2,553
essv16877856	deletion	SAMN01761612	Sequencing	Read depth and paired-end mapping	Heterozygous	2,789
essv16877857	deletion	SAMN01761624	Sequencing	Read depth and paired-end mapping	Homozygous	2,255
essv16877858	deletion	SAMN00006378	Sequencing	Read depth and paired-end mapping	Homozygous	2,702
essv16877859	deletion	SAMN00006385	Sequencing	Read depth and paired-end mapping	Heterozygous	2,419
essv16877860	deletion	SAMN00006387	Sequencing	Read depth and paired-end mapping	Heterozygous	2,527
essv16877861	deletion	SAMN00006388	Sequencing	Read depth and paired-end mapping	Heterozygous	2,552
essv16877862	deletion	SAMN00009104	Sequencing	Read depth and paired-end mapping	Heterozygous	2,613
essv16877863	deletion	SAMN00009106	Sequencing	Read depth and paired-end mapping	Heterozygous	2,582
essv16877864	deletion	SAMN00006390	Sequencing	Read depth and paired-end mapping	Heterozygous	2,374
essv16877865	deletion	SAMN00006391	Sequencing	Read depth and paired-end mapping	Homozygous	2,641
essv16877866	deletion	SAMN00009108	Sequencing	Read depth and paired-end mapping	Heterozygous	2,494
essv16877867	deletion	SAMN00006396	Sequencing	Read depth and paired-end mapping	Heterozygous	2,475
essv16877868	deletion	SAMN00006397	Sequencing	Read depth and paired-end mapping	Heterozygous	2,768
essv16877869	deletion	SAMN00006401	Sequencing	Read depth and paired-end mapping	Heterozygous	2,746
essv16877870	deletion	SAMN00006402	Sequencing	Read depth and paired-end mapping	Heterozygous	2,495
essv16877871	deletion	SAMN00006404	Sequencing	Read depth and paired-end mapping	Heterozygous	2,621
essv16877872	deletion	SAMN00006405	Sequencing	Read depth and paired-end mapping	Heterozygous	2,856
essv16877873	deletion	SAMN00006407	Sequencing	Read depth and paired-end mapping	Heterozygous	2,626
essv16877874	deletion	SAMN00006409	Sequencing	Read depth and paired-end mapping	Heterozygous	2,477
essv16877875	deletion	SAMN00006411	Sequencing	Read depth and paired-end mapping	Heterozygous	2,770
essv16877876	deletion	SAMN00006414	Sequencing	Read depth and paired-end mapping	Heterozygous	2,676
essv16877877	deletion	SAMN00006415	Sequencing	Read depth and paired-end mapping	Heterozygous	2,782
essv16877878	deletion	SAMN00006416	Sequencing	Read depth and paired-end mapping	Heterozygous	2,728
essv16877879	deletion	SAMN00006420	Sequencing	Read depth and paired-end mapping	Heterozygous	2,805
essv16877880	deletion	SAMN00006421	Sequencing	Read depth and paired-end mapping	Heterozygous	2,532
essv16877881	deletion	SAMN00006424	Sequencing	Read depth and paired-end mapping	Heterozygous	2,745
essv16877882	deletion	SAMN00006427	Sequencing	Read depth and paired-end mapping	Heterozygous	2,683
essv16877883	deletion	SAMN00006428	Sequencing	Read depth and paired-end mapping	Heterozygous	2,754
essv16877884	deletion	SAMN00006430	Sequencing	Read depth and paired-end mapping	Heterozygous	2,724
essv16877885	deletion	SAMN01036839	Sequencing	Read depth and paired-end mapping	Heterozygous	2,722
essv16877886	deletion	SAMN00004690	Sequencing	Read depth and paired-end mapping	Heterozygous	2,558
essv16877887	deletion	SAMN00006454	Sequencing	Read depth and paired-end mapping	Heterozygous	2,876
essv16877888	deletion	SAMN00006456	Sequencing	Read depth and paired-end mapping	Heterozygous	2,826
essv16877889	deletion	SAMN00006469	Sequencing	Read depth and paired-end mapping	Heterozygous	2,809
essv16877890	deletion	SAMN00006472	Sequencing	Read depth and paired-end mapping	Heterozygous	2,390
essv16877891	deletion	SAMN00006475	Sequencing	Read depth and paired-end mapping	Heterozygous	2,614
essv16877892	deletion	SAMN00006502	Sequencing	Read depth and paired-end mapping	Heterozygous	2,643
essv16877893	deletion	SAMN00006508	Sequencing	Read depth and paired-end mapping	Heterozygous	2,890
essv16877894	deletion	SAMN00006511	Sequencing	Read depth and paired-end mapping	Heterozygous	2,127
essv16877895	deletion	SAMN00006529	Sequencing	Read depth and paired-end mapping	Heterozygous	2,283
essv16877896	deletion	SAMN00006547	Sequencing	Read depth and paired-end mapping	Heterozygous	2,659
essv16877897	deletion	SAMN00006558	Sequencing	Read depth and paired-end mapping	Heterozygous	2,730
essv16877898	deletion	SAMN00006559	Sequencing	Read depth and paired-end mapping	Heterozygous	2,649
essv16877899	deletion	SAMN00006570	Sequencing	Read depth and paired-end mapping	Heterozygous	2,717
essv16877900	deletion	SAMN00249886	Sequencing	Read depth and paired-end mapping	Heterozygous	2,898
essv16877901	deletion	SAMN00249895	Sequencing	Read depth and paired-end mapping	Heterozygous	2,763
essv16877902	deletion	SAMN00249901	Sequencing	Read depth and paired-end mapping	Heterozygous	2,694
essv16877903	deletion	SAMN01091081	Sequencing	Read depth and paired-end mapping	Heterozygous	2,380
essv16877904	deletion	SAMN01091084	Sequencing	Read depth and paired-end mapping	Heterozygous	2,194
essv16877905	deletion	SAMN00009207	Sequencing	Read depth and paired-end mapping	Heterozygous	2,284
essv16877906	deletion	SAMN00009214	Sequencing	Read depth and paired-end mapping	Heterozygous	2,816
essv16877907	deletion	SAMN00009245	Sequencing	Read depth and paired-end mapping	Heterozygous	2,611
essv16877908	deletion	SAMN00014324	Sequencing	Read depth and paired-end mapping	Heterozygous	3,048
essv16877909	deletion	SAMN01091094	Sequencing	Read depth and paired-end mapping	Heterozygous	2,303
essv16877910	deletion	SAMN01091115	Sequencing	Read depth and paired-end mapping	Heterozygous	2,894
essv16877911	deletion	SAMN00014332	Sequencing	Read depth and paired-end mapping	Heterozygous	2,788
essv16877912	deletion	SAMN00014377	Sequencing	Read depth and paired-end mapping	Heterozygous	2,264
essv16877913	deletion	SAMN00014378	Sequencing	Read depth and paired-end mapping	Heterozygous	2,180
essv16877914	deletion	SAMN00014381	Sequencing	Read depth and paired-end mapping	Heterozygous	2,672
essv16877915	deletion	SAMN01761423	Sequencing	Read depth and paired-end mapping	Heterozygous	2,163
essv16877916	deletion	SAMN00014429	Sequencing	Read depth and paired-end mapping	Heterozygous	2,569
essv16877917	deletion	SAMN00016833	Sequencing	Read depth and paired-end mapping	Heterozygous	3,002
essv16877918	deletion	SAMN00263017	Sequencing	Read depth and paired-end mapping	Heterozygous	2,768
essv16877919	deletion	SAMN00255136	Sequencing	Read depth and paired-end mapping	Heterozygous	2,803
essv16877920	deletion	SAMN00249909	Sequencing	Read depth and paired-end mapping	Heterozygous	2,706
essv16877921	deletion	SAMN00249821	Sequencing	Read depth and paired-end mapping	Heterozygous	2,731
essv16877922	deletion	SAMN00249823	Sequencing	Read depth and paired-end mapping	Heterozygous	2,671
essv16877923	deletion	SAMN00249845	Sequencing	Read depth and paired-end mapping	Heterozygous	2,593
essv16877924	deletion	SAMN00249697	Sequencing	Read depth and paired-end mapping	Heterozygous	2,718
essv16877925	deletion	SAMN00249781	Sequencing	Read depth and paired-end mapping	Heterozygous	2,772
essv16877926	deletion	SAMN00263028	Sequencing	Read depth and paired-end mapping	Heterozygous	2,774
essv16877927	deletion	SAMN00630261	Sequencing	Read depth and paired-end mapping	Heterozygous	2,603
essv16877928	deletion	SAMN00249790	Sequencing	Read depth and paired-end mapping	Heterozygous	2,538
essv16877929	deletion	SAMN00249854	Sequencing	Read depth and paired-end mapping	Heterozygous	2,541
essv16877930	deletion	SAMN00249858	Sequencing	Read depth and paired-end mapping	Heterozygous	2,739
essv16877931	deletion	SAMN00249936	Sequencing	Read depth and paired-end mapping	Heterozygous	2,672
essv16877932	deletion	SAMN00255142	Sequencing	Read depth and paired-end mapping	Heterozygous	2,724
essv16877933	deletion	SAMN00263032	Sequencing	Read depth and paired-end mapping	Heterozygous	2,849
essv16877934	deletion	SAMN00263040	Sequencing	Read depth and paired-end mapping	Heterozygous	2,809
essv16877935	deletion	SAMN00263050	Sequencing	Read depth and paired-end mapping	Heterozygous	2,870
essv16877936	deletion	SAMN01091164	Sequencing	Read depth and paired-end mapping	Heterozygous	2,889
essv16877937	deletion	SAMN01091051	Sequencing	Read depth and paired-end mapping	Heterozygous	3,290

Showing 100 of 188

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv16877838	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877839	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877840	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877841	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877842	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877843	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877844	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877845	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877846	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877847	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877848	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877849	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877850	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877851	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877852	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877853	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877854	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877855	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877856	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877857	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877858	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877859	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877860	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877861	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877862	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877863	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877864	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877865	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877866	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877867	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877868	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877869	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877870	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877871	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877872	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877873	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877874	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877875	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877876	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877877	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877878	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877879	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877880	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877881	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877882	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877883	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877884	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877885	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877886	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877887	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877888	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877889	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877890	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877891	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877892	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877893	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877894	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877895	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877896	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877897	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877898	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877899	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877900	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877901	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877902	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877903	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877904	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877905	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877906	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877907	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877908	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877909	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877910	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877911	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877912	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877913	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877914	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877915	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877916	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877917	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877918	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877919	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877920	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877921	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877922	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877923	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877924	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877925	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877926	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877927	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877928	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877929	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877930	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877931	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877932	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877933	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877934	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877935	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877936	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)
essv16877937	Remapped	Perfect	NC_000023.11:g.(78 2589_782938)_(7856 69_786026)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	782,938 (-349, +0)	785,669 (-0, +357)

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dbVar

Database of genomic structural variation

esv3817503

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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.