esv3817511

Organism: Homo sapiens

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

Variant Calls:84
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: 412 SVs from 27 studies. See in: genome view

Remapped(Score: Perfect):136,033,604-136,033,604

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3817511	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
esv3817511	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000023.10	ChrX	135,115,763	135,115,763

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
essv16879378	delins	SAMN00004622	Sequencing	Read depth and paired-end mapping	Heterozygous	2,214
essv16879379	delins	SAMN00004632	Sequencing	Read depth and paired-end mapping	Heterozygous	2,666
essv16879380	delins	SAMN00004638	Sequencing	Read depth and paired-end mapping	Heterozygous	2,504
essv16879381	delins	SAMN00006339	Sequencing	Read depth and paired-end mapping	Homozygous	2,741
essv16879382	delins	SAMN00004646	Sequencing	Read depth and paired-end mapping	Heterozygous	2,568
essv16879383	delins	SAMN00016969	Sequencing	Read depth and paired-end mapping	Heterozygous	2,443
essv16879384	delins	SAMN00016972	Sequencing	Read depth and paired-end mapping	Heterozygous	2,408
essv16879385	delins	SAMN00006346	Sequencing	Read depth and paired-end mapping	Heterozygous	2,602
essv16879386	delins	SAMN00009095	Sequencing	Read depth and paired-end mapping	Heterozygous	2,620
essv16879387	delins	SAMN00006380	Sequencing	Read depth and paired-end mapping	Heterozygous	2,770
essv16879388	delins	SAMN00006381	Sequencing	Read depth and paired-end mapping	Heterozygous	2,721
essv16879389	delins	SAMN00009104	Sequencing	Read depth and paired-end mapping	Heterozygous	2,613
essv16879390	delins	SAMN00009105	Sequencing	Read depth and paired-end mapping	Heterozygous	2,596
essv16879391	delins	SAMN00006391	Sequencing	Read depth and paired-end mapping	Homozygous	2,641
essv16879392	delins	SAMN00009109	Sequencing	Read depth and paired-end mapping	Heterozygous	2,667
essv16879393	delins	SAMN00009112	Sequencing	Read depth and paired-end mapping	Heterozygous	2,788
essv16879394	delins	SAMN00006401	Sequencing	Read depth and paired-end mapping	Heterozygous	2,746
essv16879395	delins	SAMN00006404	Sequencing	Read depth and paired-end mapping	Heterozygous	2,621
essv16879396	delins	SAMN00006426	Sequencing	Read depth and paired-end mapping	Heterozygous	2,779
essv16879397	delins	SAMN00006428	Sequencing	Read depth and paired-end mapping	Heterozygous	2,754
essv16879398	delins	SAMN00006579	Sequencing	Read depth and paired-end mapping	Heterozygous	2,901
essv16879399	delins	SAMN01091079	Sequencing	Read depth and paired-end mapping	Heterozygous	2,318
essv16879400	delins	SAMN00006595	Sequencing	Read depth and paired-end mapping	Heterozygous	2,718
essv16879401	delins	SAMN01091102	Sequencing	Read depth and paired-end mapping	Heterozygous	2,849
essv16879402	delins	SAMN00009156	Sequencing	Read depth and paired-end mapping	Heterozygous	2,908
essv16879403	delins	SAMN00009193	Sequencing	Read depth and paired-end mapping	Heterozygous	2,592
essv16879404	delins	SAMN00009204	Sequencing	Read depth and paired-end mapping	Heterozygous	2,232
essv16879405	delins	SAMN00014315	Sequencing	Read depth and paired-end mapping	Heterozygous	2,643
essv16879406	delins	SAMN00014318	Sequencing	Read depth and paired-end mapping	Heterozygous	2,631
essv16879407	delins	SAMN00014320	Sequencing	Read depth and paired-end mapping	Heterozygous	2,656
essv16879408	delins	SAMN00014336	Sequencing	Read depth and paired-end mapping	Heterozygous	2,501
essv16879409	delins	SAMN00014345	Sequencing	Read depth and paired-end mapping	Heterozygous	2,610
essv16879410	delins	SAMN00014390	Sequencing	Read depth and paired-end mapping	Heterozygous	2,690
essv16879411	delins	SAMN00014435	Sequencing	Read depth and paired-end mapping	Heterozygous	2,745
essv16879412	delins	SAMN01761627	Sequencing	Read depth and paired-end mapping	Heterozygous	2,762
essv16879413	delins	SAMN00249884	Sequencing	Read depth and paired-end mapping	Heterozygous	2,705
essv16879414	delins	SAMN00249681	Sequencing	Read depth and paired-end mapping	Heterozygous	2,621
essv16879415	delins	SAMN00249687	Sequencing	Read depth and paired-end mapping	Heterozygous	2,706
essv16879416	delins	SAMN00249711	Sequencing	Read depth and paired-end mapping	Heterozygous	2,674
essv16879417	delins	SAMN00249729	Sequencing	Read depth and paired-end mapping	Heterozygous	2,417
essv16879418	delins	SAMN00630209	Sequencing	Read depth and paired-end mapping	Homozygous	3,050
essv16879419	delins	SAMN01091139	Sequencing	Read depth and paired-end mapping	Heterozygous	2,712
essv16879420	delins	SAMN01091141	Sequencing	Read depth and paired-end mapping	Heterozygous	2,624
essv16879421	delins	SAMN01761365	Sequencing	Read depth and paired-end mapping	Heterozygous	2,771
essv16879422	delins	SAMN00780000	Sequencing	Read depth and paired-end mapping	Heterozygous	2,757
essv16879423	delins	SAMN00780005	Sequencing	Read depth and paired-end mapping	Heterozygous	2,744
essv16879424	delins	SAMN00780008	Sequencing	Read depth and paired-end mapping	Heterozygous	2,701
essv16879425	delins	SAMN00780015	Sequencing	Read depth and paired-end mapping	Heterozygous	2,784
essv16879426	delins	SAMN01036834	Sequencing	Read depth and paired-end mapping	Heterozygous	2,761
essv16879427	delins	SAMN01090925	Sequencing	Read depth and paired-end mapping	Heterozygous	2,848
essv16879428	delins	SAMN01761389	Sequencing	Read depth and paired-end mapping	Heterozygous	2,211
essv16879429	delins	SAMN01091013	Sequencing	Read depth and paired-end mapping	Heterozygous	2,807
essv16879430	delins	SAMN01096741	Sequencing	Read depth and paired-end mapping	Homozygous	2,598
essv16879431	delins	SAMN01090990	Sequencing	Read depth and paired-end mapping	Heterozygous	2,766
essv16879432	delins	SAMN01091024	Sequencing	Read depth and paired-end mapping	Heterozygous	2,761
essv16879433	delins	SAMN01096689	Sequencing	Read depth and paired-end mapping	Heterozygous	2,632
essv16879434	delins	SAMN01096749	Sequencing	Read depth and paired-end mapping	Heterozygous	2,710
essv16879435	delins	SAMN01091029	Sequencing	Read depth and paired-end mapping	Heterozygous	2,716
essv16879436	delins	SAMN01096799	Sequencing	Read depth and paired-end mapping	Heterozygous	2,519
essv16879437	delins	SAMN01761570	Sequencing	Read depth and paired-end mapping	Heterozygous	2,245
essv16879438	delins	SAMN01761485	Sequencing	Read depth and paired-end mapping	Heterozygous	2,931
essv16879439	delins	SAMN01761495	Sequencing	Read depth and paired-end mapping	Heterozygous	2,858
essv16879440	delins	SAMN01761582	Sequencing	Read depth and paired-end mapping	Homozygous	2,801
essv16879441	delins	SAMN01761591	Sequencing	Read depth and paired-end mapping	Heterozygous	2,893
essv16879442	delins	SAMN00800258	Sequencing	Read depth and paired-end mapping	Heterozygous	2,935
essv16879443	delins	SAMN00801708	Sequencing	Read depth and paired-end mapping	Heterozygous	2,907
essv16879444	delins	SAMN00001564	Sequencing	Read depth and paired-end mapping	Heterozygous	2,923
essv16879445	delins	SAMN00000411	Sequencing	Read depth and paired-end mapping	Heterozygous	2,627
essv16879446	delins	SAMN00007759	Sequencing	Read depth and paired-end mapping	Heterozygous	2,116
essv16879447	delins	SAMN00007773	Sequencing	Read depth and paired-end mapping	Heterozygous	2,169
essv16879448	delins	SAMN00007776	Sequencing	Read depth and paired-end mapping	Heterozygous	2,177
essv16879449	delins	SAMN00001222	Sequencing	Read depth and paired-end mapping	Heterozygous	2,428
essv16879450	delins	SAMN00001223	Sequencing	Read depth and paired-end mapping	Heterozygous	2,705
essv16879451	delins	SAMN00001234	Sequencing	Read depth and paired-end mapping	Heterozygous	2,744
essv16879452	delins	SAMN00001252	Sequencing	Read depth and paired-end mapping	Heterozygous	3,317
essv16879453	delins	SAMN00001288	Sequencing	Read depth and paired-end mapping	Homozygous	2,516
essv16879454	delins	SAMN00001293	Sequencing	Read depth and paired-end mapping	Heterozygous	2,782
essv16879455	delins	SAMN00001331	Sequencing	Read depth and paired-end mapping	Heterozygous	2,905
essv16879456	delins	SAMN00007881	Sequencing	Read depth and paired-end mapping	Heterozygous	2,794
essv16879457	delins	SAMN00007885	Sequencing	Read depth and paired-end mapping	Heterozygous	2,700
essv16879458	delins	SAMN00007916	Sequencing	Read depth and paired-end mapping	Heterozygous	2,762
essv16879459	delins	SAMN00007925	Sequencing	Read depth and paired-end mapping	Heterozygous	2,821
essv16879460	delins	SAMN00007939	Sequencing	Read depth and paired-end mapping	Heterozygous	2,315
essv16879461	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
essv16879378	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879379	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879380	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879381	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879382	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879383	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879384	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879385	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879386	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879387	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879388	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879389	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879390	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879391	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879392	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879393	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879394	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879395	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879396	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879397	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879398	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879399	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879400	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879401	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879402	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879403	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879404	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879405	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879406	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879407	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879408	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879409	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879410	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879411	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879412	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879413	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879414	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879415	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879416	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879417	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879418	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879419	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879420	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879421	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879422	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879423	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879424	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879425	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879426	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879427	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879428	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879429	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879430	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879431	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879432	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879433	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879434	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879435	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879436	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879437	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879438	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879439	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879440	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879441	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879442	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879443	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879444	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879445	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879446	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879447	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879448	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879449	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879450	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879451	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879452	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879453	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879454	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879455	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879456	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879457	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879458	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879459	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879460	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879461	Remapped	Perfect	NC_000023.11:g.136 033604delins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	136,033,604	136,033,604
essv16879378	Submitted genomic		NC_000023.10:g.135 115763delins?	GRCh37 (hg19)		NC_000023.10	ChrX	135,115,763	135,115,763
essv16879379	Submitted genomic		NC_000023.10:g.135 115763delins?	GRCh37 (hg19)		NC_000023.10	ChrX	135,115,763	135,115,763
essv16879380	Submitted genomic		NC_000023.10:g.135 115763delins?	GRCh37 (hg19)		NC_000023.10	ChrX	135,115,763	135,115,763
essv16879381	Submitted genomic		NC_000023.10:g.135 115763delins?	GRCh37 (hg19)		NC_000023.10	ChrX	135,115,763	135,115,763
essv16879382	Submitted genomic		NC_000023.10:g.135 115763delins?	GRCh37 (hg19)		NC_000023.10	ChrX	135,115,763	135,115,763
essv16879383	Submitted genomic		NC_000023.10:g.135 115763delins?	GRCh37 (hg19)		NC_000023.10	ChrX	135,115,763	135,115,763
essv16879384	Submitted genomic		NC_000023.10:g.135 115763delins?	GRCh37 (hg19)		NC_000023.10	ChrX	135,115,763	135,115,763
essv16879385	Submitted genomic		NC_000023.10:g.135 115763delins?	GRCh37 (hg19)		NC_000023.10	ChrX	135,115,763	135,115,763
essv16879386	Submitted genomic		NC_000023.10:g.135 115763delins?	GRCh37 (hg19)		NC_000023.10	ChrX	135,115,763	135,115,763
essv16879387	Submitted genomic		NC_000023.10:g.135 115763delins?	GRCh37 (hg19)		NC_000023.10	ChrX	135,115,763	135,115,763
essv16879388	Submitted genomic		NC_000023.10:g.135 115763delins?	GRCh37 (hg19)		NC_000023.10	ChrX	135,115,763	135,115,763
essv16879389	Submitted genomic		NC_000023.10:g.135 115763delins?	GRCh37 (hg19)		NC_000023.10	ChrX	135,115,763	135,115,763
essv16879390	Submitted genomic		NC_000023.10:g.135 115763delins?	GRCh37 (hg19)		NC_000023.10	ChrX	135,115,763	135,115,763
essv16879391	Submitted genomic		NC_000023.10:g.135 115763delins?	GRCh37 (hg19)		NC_000023.10	ChrX	135,115,763	135,115,763
essv16879392	Submitted genomic		NC_000023.10:g.135 115763delins?	GRCh37 (hg19)		NC_000023.10	ChrX	135,115,763	135,115,763
essv16879393	Submitted genomic		NC_000023.10:g.135 115763delins?	GRCh37 (hg19)		NC_000023.10	ChrX	135,115,763	135,115,763

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dbVar

Database of genomic structural variation

esv3817511

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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.