esv3647660

Organism: Homo sapiens

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

Variant Calls:46
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: 86 SVs from 22 studies. See in: genome view

Remapped(Score: Perfect):35,189,474-35,189,474

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3647660	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000022.11	Chr22	35,189,474	35,189,474
esv3647660	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000022.10	Chr22	35,585,467	35,585,467

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
essv16411337	sva insertion	SAMN00014426	Sequencing	Read depth and paired-end mapping	Heterozygous	2,577
essv16411338	sva insertion	SAMN00262993	Sequencing	Read depth and paired-end mapping	Heterozygous	3,311
essv16411339	sva insertion	SAMN00630198	Sequencing	Read depth and paired-end mapping	Heterozygous	3,096
essv16411340	sva insertion	SAMN00262992	Sequencing	Read depth and paired-end mapping	Heterozygous	3,290
essv16411341	sva insertion	SAMN00262972	Sequencing	Read depth and paired-end mapping	Heterozygous	3,149
essv16411342	sva insertion	SAMN00630236	Sequencing	Read depth and paired-end mapping	Heterozygous	3,237
essv16411343	sva insertion	SAMN01091055	Sequencing	Read depth and paired-end mapping	Heterozygous	3,351
essv16411344	sva insertion	SAMN00779940	Sequencing	Read depth and paired-end mapping	Heterozygous	3,140
essv16411345	sva insertion	SAMN00779954	Sequencing	Read depth and paired-end mapping	Heterozygous	3,099
essv16411346	sva insertion	SAMN00779960	Sequencing	Read depth and paired-end mapping	Heterozygous	3,258
essv16411347	sva insertion	SAMN00779988	Sequencing	Read depth and paired-end mapping	Heterozygous	3,242
essv16411348	sva insertion	SAMN01036725	Sequencing	Read depth and paired-end mapping	Heterozygous	3,135
essv16411349	sva insertion	SAMN01090862	Sequencing	Read depth and paired-end mapping	Homozygous	2,935
essv16411350	sva insertion	SAMN01761280	Sequencing	Read depth and paired-end mapping	Heterozygous	3,222
essv16411351	sva insertion	SAMN01090871	Sequencing	Read depth and paired-end mapping	Heterozygous	2,942
essv16411352	sva insertion	SAMN01036751	Sequencing	Read depth and paired-end mapping	Heterozygous	3,200
essv16411353	sva insertion	SAMN01761245	Sequencing	Read depth and paired-end mapping	Heterozygous	3,282
essv16411354	sva insertion	SAMN01761295	Sequencing	Read depth and paired-end mapping	Heterozygous	3,217
essv16411355	sva insertion	SAMN01090883	Sequencing	Read depth and paired-end mapping	Heterozygous	3,017
essv16411356	sva insertion	SAMN01090886	Sequencing	Read depth and paired-end mapping	Heterozygous	3,245
essv16411357	sva insertion	SAMN01036757	Sequencing	Read depth and paired-end mapping	Heterozygous	3,215
essv16411358	sva insertion	SAMN01036758	Sequencing	Read depth and paired-end mapping	Heterozygous	2,993
essv16411359	sva insertion	SAMN01090846	Sequencing	Read depth and paired-end mapping	Heterozygous	3,080
essv16411360	sva insertion	SAMN01090853	Sequencing	Read depth and paired-end mapping	Heterozygous	2,890
essv16411361	sva insertion	SAMN01761323	Sequencing	Read depth and paired-end mapping	Heterozygous	3,121
essv16411362	sva insertion	SAMN01090818	Sequencing	Read depth and paired-end mapping	Heterozygous	3,288
essv16411363	sva insertion	SAMN01036791	Sequencing	Read depth and paired-end mapping	Heterozygous	3,202
essv16411364	sva insertion	SAMN01090769	Sequencing	Read depth and paired-end mapping	Heterozygous	2,975
essv16411365	sva insertion	SAMN01761348	Sequencing	Read depth and paired-end mapping	Heterozygous	3,263
essv16411366	sva insertion	SAMN01761350	Sequencing	Read depth and paired-end mapping	Heterozygous	2,677
essv16411367	sva insertion	SAMN00001577	Sequencing	Read depth and paired-end mapping	Heterozygous	3,105
essv16411368	sva insertion	SAMN00001051	Sequencing	Read depth and paired-end mapping	Heterozygous	2,862
essv16411369	sva insertion	SAMN00001054	Sequencing	Read depth and paired-end mapping	Heterozygous	3,219
essv16411370	sva insertion	SAMN00001057	Sequencing	Read depth and paired-end mapping	Heterozygous	3,084
essv16411371	sva insertion	SAMN00001059	Sequencing	Read depth and paired-end mapping	Heterozygous	3,175
essv16411372	sva insertion	SAMN00000547	Sequencing	Read depth and paired-end mapping	Heterozygous	3,222
essv16411373	sva insertion	SAMN00001104	Sequencing	Read depth and paired-end mapping	Heterozygous	2,712
essv16411374	sva insertion	SAMN00001110	Sequencing	Read depth and paired-end mapping	Heterozygous	3,124
essv16411375	sva insertion	SAMN00001119	Sequencing	Read depth and paired-end mapping	Heterozygous	3,113
essv16411376	sva insertion	SAMN00001131	Sequencing	Read depth and paired-end mapping	Heterozygous	3,007
essv16411377	sva insertion	SAMN00001132	Sequencing	Read depth and paired-end mapping	Heterozygous	2,992
essv16411378	sva insertion	SAMN00001174	Sequencing	Read depth and paired-end mapping	Heterozygous	2,734
essv16411379	sva insertion	SAMN00001179	Sequencing	Read depth and paired-end mapping	Heterozygous	3,049
essv16411380	sva insertion	SAMN00001191	Sequencing	Read depth and paired-end mapping	Heterozygous	2,982
essv16411381	sva insertion	SAMN00007700	Sequencing	Read depth and paired-end mapping	Heterozygous	3,096
essv16411382	sva insertion	SAMN00007874	Sequencing	Read depth and paired-end mapping	Heterozygous	3,150

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv16411337	Remapped	Perfect	NC_000022.11:g.351 89474_35189475ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	35,189,474	35,189,474
essv16411338	Remapped	Perfect	NC_000022.11:g.351 89474_35189475ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	35,189,474	35,189,474
essv16411339	Remapped	Perfect	NC_000022.11:g.351 89474_35189475ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	35,189,474	35,189,474
essv16411340	Remapped	Perfect	NC_000022.11:g.351 89474_35189475ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	35,189,474	35,189,474
essv16411341	Remapped	Perfect	NC_000022.11:g.351 89474_35189475ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	35,189,474	35,189,474
essv16411342	Remapped	Perfect	NC_000022.11:g.351 89474_35189475ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	35,189,474	35,189,474
essv16411343	Remapped	Perfect	NC_000022.11:g.351 89474_35189475ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	35,189,474	35,189,474
essv16411344	Remapped	Perfect	NC_000022.11:g.351 89474_35189475ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	35,189,474	35,189,474
essv16411345	Remapped	Perfect	NC_000022.11:g.351 89474_35189475ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	35,189,474	35,189,474
essv16411346	Remapped	Perfect	NC_000022.11:g.351 89474_35189475ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	35,189,474	35,189,474
essv16411347	Remapped	Perfect	NC_000022.11:g.351 89474_35189475ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	35,189,474	35,189,474
essv16411348	Remapped	Perfect	NC_000022.11:g.351 89474_35189475ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	35,189,474	35,189,474
essv16411349	Remapped	Perfect	NC_000022.11:g.351 89474_35189475ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	35,189,474	35,189,474
essv16411350	Remapped	Perfect	NC_000022.11:g.351 89474_35189475ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	35,189,474	35,189,474
essv16411351	Remapped	Perfect	NC_000022.11:g.351 89474_35189475ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	35,189,474	35,189,474
essv16411352	Remapped	Perfect	NC_000022.11:g.351 89474_35189475ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	35,189,474	35,189,474
essv16411353	Remapped	Perfect	NC_000022.11:g.351 89474_35189475ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	35,189,474	35,189,474
essv16411354	Remapped	Perfect	NC_000022.11:g.351 89474_35189475ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	35,189,474	35,189,474
essv16411355	Remapped	Perfect	NC_000022.11:g.351 89474_35189475ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	35,189,474	35,189,474
essv16411356	Remapped	Perfect	NC_000022.11:g.351 89474_35189475ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	35,189,474	35,189,474
essv16411357	Remapped	Perfect	NC_000022.11:g.351 89474_35189475ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	35,189,474	35,189,474
essv16411358	Remapped	Perfect	NC_000022.11:g.351 89474_35189475ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	35,189,474	35,189,474
essv16411359	Remapped	Perfect	NC_000022.11:g.351 89474_35189475ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	35,189,474	35,189,474
essv16411360	Remapped	Perfect	NC_000022.11:g.351 89474_35189475ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	35,189,474	35,189,474
essv16411361	Remapped	Perfect	NC_000022.11:g.351 89474_35189475ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	35,189,474	35,189,474
essv16411362	Remapped	Perfect	NC_000022.11:g.351 89474_35189475ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	35,189,474	35,189,474
essv16411363	Remapped	Perfect	NC_000022.11:g.351 89474_35189475ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	35,189,474	35,189,474
essv16411364	Remapped	Perfect	NC_000022.11:g.351 89474_35189475ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	35,189,474	35,189,474
essv16411365	Remapped	Perfect	NC_000022.11:g.351 89474_35189475ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	35,189,474	35,189,474
essv16411366	Remapped	Perfect	NC_000022.11:g.351 89474_35189475ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	35,189,474	35,189,474
essv16411367	Remapped	Perfect	NC_000022.11:g.351 89474_35189475ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	35,189,474	35,189,474
essv16411368	Remapped	Perfect	NC_000022.11:g.351 89474_35189475ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	35,189,474	35,189,474
essv16411369	Remapped	Perfect	NC_000022.11:g.351 89474_35189475ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	35,189,474	35,189,474
essv16411370	Remapped	Perfect	NC_000022.11:g.351 89474_35189475ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	35,189,474	35,189,474
essv16411371	Remapped	Perfect	NC_000022.11:g.351 89474_35189475ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	35,189,474	35,189,474
essv16411372	Remapped	Perfect	NC_000022.11:g.351 89474_35189475ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	35,189,474	35,189,474
essv16411373	Remapped	Perfect	NC_000022.11:g.351 89474_35189475ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	35,189,474	35,189,474
essv16411374	Remapped	Perfect	NC_000022.11:g.351 89474_35189475ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	35,189,474	35,189,474
essv16411375	Remapped	Perfect	NC_000022.11:g.351 89474_35189475ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	35,189,474	35,189,474
essv16411376	Remapped	Perfect	NC_000022.11:g.351 89474_35189475ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	35,189,474	35,189,474
essv16411377	Remapped	Perfect	NC_000022.11:g.351 89474_35189475ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	35,189,474	35,189,474
essv16411378	Remapped	Perfect	NC_000022.11:g.351 89474_35189475ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	35,189,474	35,189,474
essv16411379	Remapped	Perfect	NC_000022.11:g.351 89474_35189475ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	35,189,474	35,189,474
essv16411380	Remapped	Perfect	NC_000022.11:g.351 89474_35189475ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	35,189,474	35,189,474
essv16411381	Remapped	Perfect	NC_000022.11:g.351 89474_35189475ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	35,189,474	35,189,474
essv16411382	Remapped	Perfect	NC_000022.11:g.351 89474_35189475ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	35,189,474	35,189,474
essv16411337	Submitted genomic		NC_000022.10:g.355 85467_35585468ins?	GRCh37 (hg19)		NC_000022.10	Chr22	35,585,467	35,585,467
essv16411338	Submitted genomic		NC_000022.10:g.355 85467_35585468ins?	GRCh37 (hg19)		NC_000022.10	Chr22	35,585,467	35,585,467
essv16411339	Submitted genomic		NC_000022.10:g.355 85467_35585468ins?	GRCh37 (hg19)		NC_000022.10	Chr22	35,585,467	35,585,467
essv16411340	Submitted genomic		NC_000022.10:g.355 85467_35585468ins?	GRCh37 (hg19)		NC_000022.10	Chr22	35,585,467	35,585,467
essv16411341	Submitted genomic		NC_000022.10:g.355 85467_35585468ins?	GRCh37 (hg19)		NC_000022.10	Chr22	35,585,467	35,585,467
essv16411342	Submitted genomic		NC_000022.10:g.355 85467_35585468ins?	GRCh37 (hg19)		NC_000022.10	Chr22	35,585,467	35,585,467
essv16411343	Submitted genomic		NC_000022.10:g.355 85467_35585468ins?	GRCh37 (hg19)		NC_000022.10	Chr22	35,585,467	35,585,467
essv16411344	Submitted genomic		NC_000022.10:g.355 85467_35585468ins?	GRCh37 (hg19)		NC_000022.10	Chr22	35,585,467	35,585,467
essv16411345	Submitted genomic		NC_000022.10:g.355 85467_35585468ins?	GRCh37 (hg19)		NC_000022.10	Chr22	35,585,467	35,585,467
essv16411346	Submitted genomic		NC_000022.10:g.355 85467_35585468ins?	GRCh37 (hg19)		NC_000022.10	Chr22	35,585,467	35,585,467
essv16411347	Submitted genomic		NC_000022.10:g.355 85467_35585468ins?	GRCh37 (hg19)		NC_000022.10	Chr22	35,585,467	35,585,467
essv16411348	Submitted genomic		NC_000022.10:g.355 85467_35585468ins?	GRCh37 (hg19)		NC_000022.10	Chr22	35,585,467	35,585,467
essv16411349	Submitted genomic		NC_000022.10:g.355 85467_35585468ins?	GRCh37 (hg19)		NC_000022.10	Chr22	35,585,467	35,585,467
essv16411350	Submitted genomic		NC_000022.10:g.355 85467_35585468ins?	GRCh37 (hg19)		NC_000022.10	Chr22	35,585,467	35,585,467
essv16411351	Submitted genomic		NC_000022.10:g.355 85467_35585468ins?	GRCh37 (hg19)		NC_000022.10	Chr22	35,585,467	35,585,467
essv16411352	Submitted genomic		NC_000022.10:g.355 85467_35585468ins?	GRCh37 (hg19)		NC_000022.10	Chr22	35,585,467	35,585,467
essv16411353	Submitted genomic		NC_000022.10:g.355 85467_35585468ins?	GRCh37 (hg19)		NC_000022.10	Chr22	35,585,467	35,585,467
essv16411354	Submitted genomic		NC_000022.10:g.355 85467_35585468ins?	GRCh37 (hg19)		NC_000022.10	Chr22	35,585,467	35,585,467
essv16411355	Submitted genomic		NC_000022.10:g.355 85467_35585468ins?	GRCh37 (hg19)		NC_000022.10	Chr22	35,585,467	35,585,467
essv16411356	Submitted genomic		NC_000022.10:g.355 85467_35585468ins?	GRCh37 (hg19)		NC_000022.10	Chr22	35,585,467	35,585,467
essv16411357	Submitted genomic		NC_000022.10:g.355 85467_35585468ins?	GRCh37 (hg19)		NC_000022.10	Chr22	35,585,467	35,585,467
essv16411358	Submitted genomic		NC_000022.10:g.355 85467_35585468ins?	GRCh37 (hg19)		NC_000022.10	Chr22	35,585,467	35,585,467
essv16411359	Submitted genomic		NC_000022.10:g.355 85467_35585468ins?	GRCh37 (hg19)		NC_000022.10	Chr22	35,585,467	35,585,467
essv16411360	Submitted genomic		NC_000022.10:g.355 85467_35585468ins?	GRCh37 (hg19)		NC_000022.10	Chr22	35,585,467	35,585,467
essv16411361	Submitted genomic		NC_000022.10:g.355 85467_35585468ins?	GRCh37 (hg19)		NC_000022.10	Chr22	35,585,467	35,585,467
essv16411362	Submitted genomic		NC_000022.10:g.355 85467_35585468ins?	GRCh37 (hg19)		NC_000022.10	Chr22	35,585,467	35,585,467
essv16411363	Submitted genomic		NC_000022.10:g.355 85467_35585468ins?	GRCh37 (hg19)		NC_000022.10	Chr22	35,585,467	35,585,467
essv16411364	Submitted genomic		NC_000022.10:g.355 85467_35585468ins?	GRCh37 (hg19)		NC_000022.10	Chr22	35,585,467	35,585,467
essv16411365	Submitted genomic		NC_000022.10:g.355 85467_35585468ins?	GRCh37 (hg19)		NC_000022.10	Chr22	35,585,467	35,585,467
essv16411366	Submitted genomic		NC_000022.10:g.355 85467_35585468ins?	GRCh37 (hg19)		NC_000022.10	Chr22	35,585,467	35,585,467
essv16411367	Submitted genomic		NC_000022.10:g.355 85467_35585468ins?	GRCh37 (hg19)		NC_000022.10	Chr22	35,585,467	35,585,467
essv16411368	Submitted genomic		NC_000022.10:g.355 85467_35585468ins?	GRCh37 (hg19)		NC_000022.10	Chr22	35,585,467	35,585,467
essv16411369	Submitted genomic		NC_000022.10:g.355 85467_35585468ins?	GRCh37 (hg19)		NC_000022.10	Chr22	35,585,467	35,585,467
essv16411370	Submitted genomic		NC_000022.10:g.355 85467_35585468ins?	GRCh37 (hg19)		NC_000022.10	Chr22	35,585,467	35,585,467
essv16411371	Submitted genomic		NC_000022.10:g.355 85467_35585468ins?	GRCh37 (hg19)		NC_000022.10	Chr22	35,585,467	35,585,467
essv16411372	Submitted genomic		NC_000022.10:g.355 85467_35585468ins?	GRCh37 (hg19)		NC_000022.10	Chr22	35,585,467	35,585,467
essv16411373	Submitted genomic		NC_000022.10:g.355 85467_35585468ins?	GRCh37 (hg19)		NC_000022.10	Chr22	35,585,467	35,585,467
essv16411374	Submitted genomic		NC_000022.10:g.355 85467_35585468ins?	GRCh37 (hg19)		NC_000022.10	Chr22	35,585,467	35,585,467
essv16411375	Submitted genomic		NC_000022.10:g.355 85467_35585468ins?	GRCh37 (hg19)		NC_000022.10	Chr22	35,585,467	35,585,467
essv16411376	Submitted genomic		NC_000022.10:g.355 85467_35585468ins?	GRCh37 (hg19)		NC_000022.10	Chr22	35,585,467	35,585,467
essv16411377	Submitted genomic		NC_000022.10:g.355 85467_35585468ins?	GRCh37 (hg19)		NC_000022.10	Chr22	35,585,467	35,585,467
essv16411378	Submitted genomic		NC_000022.10:g.355 85467_35585468ins?	GRCh37 (hg19)		NC_000022.10	Chr22	35,585,467	35,585,467
essv16411379	Submitted genomic		NC_000022.10:g.355 85467_35585468ins?	GRCh37 (hg19)		NC_000022.10	Chr22	35,585,467	35,585,467
essv16411380	Submitted genomic		NC_000022.10:g.355 85467_35585468ins?	GRCh37 (hg19)		NC_000022.10	Chr22	35,585,467	35,585,467
essv16411381	Submitted genomic		NC_000022.10:g.355 85467_35585468ins?	GRCh37 (hg19)		NC_000022.10	Chr22	35,585,467	35,585,467
essv16411382	Submitted genomic		NC_000022.10:g.355 85467_35585468ins?	GRCh37 (hg19)		NC_000022.10	Chr22	35,585,467	35,585,467

dbVar

Database of genomic structural variation

esv3647660

Links to Other Resources

Genome View

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.