esv3817791

Organism: Homo sapiens

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

Variant Calls:80
Validation:Not tested
Clinical Assertions: No
Region Size:1

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: 431 SVs from 22 studies. See in: genome view

Remapped(Score: Perfect):152,251,004-152,251,004

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3817791	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
esv3817791	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000023.10	ChrX	151,419,476	151,419,476

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
essv16920897	delins	SAMN00009108	Sequencing	Read depth and paired-end mapping	Heterozygous	2,494
essv16920898	delins	SAMN00006454	Sequencing	Read depth and paired-end mapping	Heterozygous	2,876
essv16920899	delins	SAMN00249900	Sequencing	Read depth and paired-end mapping	Heterozygous	2,715
essv16920900	delins	SAMN01091115	Sequencing	Read depth and paired-end mapping	Heterozygous	2,894
essv16920901	delins	SAMN00249938	Sequencing	Read depth and paired-end mapping	Heterozygous	2,782
essv16920902	delins	SAMN01036825	Sequencing	Read depth and paired-end mapping	Heterozygous	2,879
essv16920903	delins	SAMN01761410	Sequencing	Read depth and paired-end mapping	Heterozygous	2,225
essv16920904	delins	SAMN01761383	Sequencing	Read depth and paired-end mapping	Heterozygous	2,852
essv16920905	delins	SAMN01761430	Sequencing	Read depth and paired-end mapping	Heterozygous	2,240
essv16920906	delins	SAMN01096710	Sequencing	Read depth and paired-end mapping	Heterozygous	2,613
essv16920907	delins	SAMN01096713	Sequencing	Read depth and paired-end mapping	Heterozygous	2,561
essv16920908	delins	SAMN01761434	Sequencing	Read depth and paired-end mapping	Heterozygous	2,918
essv16920909	delins	SAMN01761414	Sequencing	Read depth and paired-end mapping	Heterozygous	2,367
essv16920910	delins	SAMN01096723	Sequencing	Read depth and paired-end mapping	Heterozygous	2,577
essv16920911	delins	SAMN01761436	Sequencing	Read depth and paired-end mapping	Heterozygous	2,919
essv16920912	delins	SAMN01090922	Sequencing	Read depth and paired-end mapping	Heterozygous	2,812
essv16920913	delins	SAMN01096727	Sequencing	Read depth and paired-end mapping	Heterozygous	2,834
essv16920914	delins	SAMN01096728	Sequencing	Read depth and paired-end mapping	Heterozygous	2,719
essv16920915	delins	SAMN01096739	Sequencing	Read depth and paired-end mapping	Heterozygous	2,582
essv16920916	delins	SAMN01761401	Sequencing	Read depth and paired-end mapping	Heterozygous	2,199
essv16920917	delins	SAMN01096740	Sequencing	Read depth and paired-end mapping	Heterozygous	2,660
essv16920918	delins	SAMN01091010	Sequencing	Read depth and paired-end mapping	Heterozygous	2,708
essv16920919	delins	SAMN01090983	Sequencing	Read depth and paired-end mapping	Heterozygous	2,841
essv16920920	delins	SAMN01096744	Sequencing	Read depth and paired-end mapping	Heterozygous	2,657
essv16920921	delins	SAMN01090987	Sequencing	Read depth and paired-end mapping	Heterozygous	2,785
essv16920922	delins	SAMN01096748	Sequencing	Read depth and paired-end mapping	Heterozygous	2,740
essv16920923	delins	SAMN01091017	Sequencing	Read depth and paired-end mapping	Heterozygous	2,778
essv16920924	delins	SAMN01091021	Sequencing	Read depth and paired-end mapping	Heterozygous	2,842
essv16920925	delins	SAMN01091028	Sequencing	Read depth and paired-end mapping	Heterozygous	2,772
essv16920926	delins	SAMN01090945	Sequencing	Read depth and paired-end mapping	Heterozygous	2,687
essv16920927	delins	SAMN01096686	Sequencing	Read depth and paired-end mapping	Heterozygous	2,657
essv16920928	delins	SAMN01090995	Sequencing	Read depth and paired-end mapping	Heterozygous	2,830
essv16920929	delins	SAMN01090997	Sequencing	Read depth and paired-end mapping	Homozygous	2,690
essv16920930	delins	SAMN01096789	Sequencing	Read depth and paired-end mapping	Heterozygous	2,597
essv16920931	delins	SAMN01090988	Sequencing	Read depth and paired-end mapping	Heterozygous	2,742
essv16920932	delins	SAMN01096718	Sequencing	Read depth and paired-end mapping	Heterozygous	2,496
essv16920933	delins	SAMN01096719	Sequencing	Read depth and paired-end mapping	Heterozygous	2,696
essv16920934	delins	SAMN01090960	Sequencing	Read depth and paired-end mapping	Heterozygous	2,611
essv16920935	delins	SAMN01096763	Sequencing	Read depth and paired-end mapping	Heterozygous	2,569
essv16920936	delins	SAMN01096793	Sequencing	Read depth and paired-end mapping	Heterozygous	2,614
essv16920937	delins	SAMN01091037	Sequencing	Read depth and paired-end mapping	Heterozygous	2,565
essv16920938	delins	SAMN01096772	Sequencing	Read depth and paired-end mapping	Heterozygous	2,611
essv16920939	delins	SAMN01096801	Sequencing	Read depth and paired-end mapping	Heterozygous	2,563
essv16920940	delins	SAMN01096777	Sequencing	Read depth and paired-end mapping	Heterozygous	2,589
essv16920941	delins	SAMN01096800	Sequencing	Read depth and paired-end mapping	Heterozygous	2,625
essv16920942	delins	SAMN01096803	Sequencing	Read depth and paired-end mapping	Heterozygous	2,810
essv16920943	delins	SAMN01096799	Sequencing	Read depth and paired-end mapping	Heterozygous	2,519
essv16920944	delins	SAMN01091041	Sequencing	Read depth and paired-end mapping	Heterozygous	2,568
essv16920945	delins	SAMN01761531	Sequencing	Read depth and paired-end mapping	Heterozygous	2,227
essv16920946	delins	SAMN01096804	Sequencing	Read depth and paired-end mapping	Heterozygous	2,549
essv16920947	delins	SAMN01761489	Sequencing	Read depth and paired-end mapping	Heterozygous	2,862
essv16920948	delins	SAMN01761475	Sequencing	Read depth and paired-end mapping	Heterozygous	3,001
essv16920949	delins	SAMN01096711	Sequencing	Read depth and paired-end mapping	Heterozygous	2,626
essv16920950	delins	SAMN01761495	Sequencing	Read depth and paired-end mapping	Heterozygous	2,858
essv16920951	delins	SAMN01761591	Sequencing	Read depth and paired-end mapping	Homozygous	2,893
essv16920952	delins	SAMN01761596	Sequencing	Read depth and paired-end mapping	Heterozygous	2,900
essv16920953	delins	SAMN00000474	Sequencing	Read depth and paired-end mapping	Heterozygous	3,015
essv16920954	delins	SAMN00001025	Sequencing	Read depth and paired-end mapping	Heterozygous	3,307
essv16920955	delins	SAMN00001629	Sequencing	Read depth and paired-end mapping	Heterozygous	3,357
essv16920956	delins	SAMN00000497	Sequencing	Read depth and paired-end mapping	Heterozygous	2,523
essv16920957	delins	SAMN00001689	Sequencing	Read depth and paired-end mapping	Heterozygous	2,573
essv16920958	delins	SAMN00000568	Sequencing	Read depth and paired-end mapping	Heterozygous	3,048
essv16920959	delins	SAMN00001697	Sequencing	Read depth and paired-end mapping	Heterozygous	3,373
essv16920960	delins	SAMN00007817	Sequencing	Read depth and paired-end mapping	Heterozygous	3,065
essv16920961	delins	SAMN00007904	Sequencing	Read depth and paired-end mapping	Homozygous	2,791
essv16920962	delins	SAMN00007909	Sequencing	Read depth and paired-end mapping	Heterozygous	2,823
essv16920963	delins	SAMN00007917	Sequencing	Read depth and paired-end mapping	Heterozygous	2,728
essv16920964	delins	SAMN00007925	Sequencing	Read depth and paired-end mapping	Heterozygous	2,821
essv16920965	delins	SAMN00007927	Sequencing	Read depth and paired-end mapping	Heterozygous	2,702
essv16920966	delins	SAMN00007937	Sequencing	Read depth and paired-end mapping	Heterozygous	2,756
essv16920967	delins	SAMN00007944	Sequencing	Read depth and paired-end mapping	Heterozygous	2,330
essv16920968	delins	SAMN00007945	Sequencing	Read depth and paired-end mapping	Heterozygous	2,490
essv16920969	delins	SAMN00007947	Sequencing	Read depth and paired-end mapping	Heterozygous	2,277
essv16920970	delins	SAMN00007953	Sequencing	Read depth and paired-end mapping	Heterozygous	2,763
essv16920971	delins	SAMN00007968	Sequencing	Read depth and paired-end mapping	Heterozygous	2,736
essv16920972	delins	SAMN00004497	Sequencing	Read depth and paired-end mapping	Heterozygous	2,798
essv16920973	delins	SAMN00007969	Sequencing	Read depth and paired-end mapping	Heterozygous	2,957
essv16920974	delins	SAMN00007974	Sequencing	Read depth and paired-end mapping	Heterozygous	2,844
essv16920975	delins	SAMN00007978	Sequencing	Read depth and paired-end mapping	Heterozygous	2,916
essv16920976	delins	SAMN00007979	Sequencing	Read depth and paired-end mapping	Heterozygous	2,822

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv16920897	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920898	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920899	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920900	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920901	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920902	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920903	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920904	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920905	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920906	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920907	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920908	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920909	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920910	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920911	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920912	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920913	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920914	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920915	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920916	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920917	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920918	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920919	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920920	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920921	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920922	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920923	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920924	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920925	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920926	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920927	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920928	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920929	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920930	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920931	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920932	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920933	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920934	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920935	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920936	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920937	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920938	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920939	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920940	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920941	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920942	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920943	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920944	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920945	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920946	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920947	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920948	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920949	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920950	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920951	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920952	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920953	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920954	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920955	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920956	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920957	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920958	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920959	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920960	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920961	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920962	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920963	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920964	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920965	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920966	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920967	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920968	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920969	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920970	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920971	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920972	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920973	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920974	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920975	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920976	Remapped	Perfect	NC_000023.11:g.152 251004delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	152,251,004	152,251,004
essv16920897	Submitted genomic		NC_000023.10:g.151 419476delins?	GRCh37 (hg19)		NC_000023.10	ChrX	151,419,476	151,419,476
essv16920898	Submitted genomic		NC_000023.10:g.151 419476delins?	GRCh37 (hg19)		NC_000023.10	ChrX	151,419,476	151,419,476
essv16920899	Submitted genomic		NC_000023.10:g.151 419476delins?	GRCh37 (hg19)		NC_000023.10	ChrX	151,419,476	151,419,476
essv16920900	Submitted genomic		NC_000023.10:g.151 419476delins?	GRCh37 (hg19)		NC_000023.10	ChrX	151,419,476	151,419,476
essv16920901	Submitted genomic		NC_000023.10:g.151 419476delins?	GRCh37 (hg19)		NC_000023.10	ChrX	151,419,476	151,419,476
essv16920902	Submitted genomic		NC_000023.10:g.151 419476delins?	GRCh37 (hg19)		NC_000023.10	ChrX	151,419,476	151,419,476
essv16920903	Submitted genomic		NC_000023.10:g.151 419476delins?	GRCh37 (hg19)		NC_000023.10	ChrX	151,419,476	151,419,476
essv16920904	Submitted genomic		NC_000023.10:g.151 419476delins?	GRCh37 (hg19)		NC_000023.10	ChrX	151,419,476	151,419,476
essv16920905	Submitted genomic		NC_000023.10:g.151 419476delins?	GRCh37 (hg19)		NC_000023.10	ChrX	151,419,476	151,419,476
essv16920906	Submitted genomic		NC_000023.10:g.151 419476delins?	GRCh37 (hg19)		NC_000023.10	ChrX	151,419,476	151,419,476
essv16920907	Submitted genomic		NC_000023.10:g.151 419476delins?	GRCh37 (hg19)		NC_000023.10	ChrX	151,419,476	151,419,476
essv16920908	Submitted genomic		NC_000023.10:g.151 419476delins?	GRCh37 (hg19)		NC_000023.10	ChrX	151,419,476	151,419,476
essv16920909	Submitted genomic		NC_000023.10:g.151 419476delins?	GRCh37 (hg19)		NC_000023.10	ChrX	151,419,476	151,419,476
essv16920910	Submitted genomic		NC_000023.10:g.151 419476delins?	GRCh37 (hg19)		NC_000023.10	ChrX	151,419,476	151,419,476
essv16920911	Submitted genomic		NC_000023.10:g.151 419476delins?	GRCh37 (hg19)		NC_000023.10	ChrX	151,419,476	151,419,476
essv16920912	Submitted genomic		NC_000023.10:g.151 419476delins?	GRCh37 (hg19)		NC_000023.10	ChrX	151,419,476	151,419,476
essv16920913	Submitted genomic		NC_000023.10:g.151 419476delins?	GRCh37 (hg19)		NC_000023.10	ChrX	151,419,476	151,419,476
essv16920914	Submitted genomic		NC_000023.10:g.151 419476delins?	GRCh37 (hg19)		NC_000023.10	ChrX	151,419,476	151,419,476
essv16920915	Submitted genomic		NC_000023.10:g.151 419476delins?	GRCh37 (hg19)		NC_000023.10	ChrX	151,419,476	151,419,476
essv16920916	Submitted genomic		NC_000023.10:g.151 419476delins?	GRCh37 (hg19)		NC_000023.10	ChrX	151,419,476	151,419,476

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dbVar

Database of genomic structural variation

esv3817791

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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.