esv3817087

Organism: Homo sapiens

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

Variant Calls:39
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: 434 SVs from 29 studies. See in: genome view

Remapped(Score: Perfect):131,096,760-131,096,760

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3817087	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000023.11	ChrX	131,096,760	131,096,760
esv3817087	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000023.10	ChrX	130,230,734	130,230,734

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
essv16812690	mobile element insertion	SAMN00006474	Sequencing	Read depth and paired-end mapping	Heterozygous	2,735
essv16812691	mobile element insertion	SAMN00006505	Sequencing	Read depth and paired-end mapping	Heterozygous	2,557
essv16812692	mobile element insertion	SAMN00006517	Sequencing	Read depth and paired-end mapping	Heterozygous	2,223
essv16812693	mobile element insertion	SAMN00249887	Sequencing	Read depth and paired-end mapping	Heterozygous	2,781
essv16812694	mobile element insertion	SAMN00249815	Sequencing	Read depth and paired-end mapping	Heterozygous	2,729
essv16812695	mobile element insertion	SAMN00016832	Sequencing	Read depth and paired-end mapping	Heterozygous	2,802
essv16812696	mobile element insertion	SAMN00249904	Sequencing	Read depth and paired-end mapping	Heterozygous	2,778
essv16812697	mobile element insertion	SAMN00249917	Sequencing	Read depth and paired-end mapping	Heterozygous	2,687
essv16812698	mobile element insertion	SAMN00249798	Sequencing	Read depth and paired-end mapping	Heterozygous	2,911
essv16812699	mobile element insertion	SAMN00255151	Sequencing	Read depth and paired-end mapping	Heterozygous	2,737
essv16812700	mobile element insertion	SAMN00249922	Sequencing	Read depth and paired-end mapping	Heterozygous	2,794
essv16812701	mobile element insertion	SAMN00249927	Sequencing	Read depth and paired-end mapping	Heterozygous	2,787
essv16812702	mobile element insertion	SAMN00249940	Sequencing	Read depth and paired-end mapping	Heterozygous	2,767
essv16812703	mobile element insertion	SAMN00263044	Sequencing	Read depth and paired-end mapping	Heterozygous	2,805
essv16812704	mobile element insertion	SAMN00779931	Sequencing	Read depth and paired-end mapping	Heterozygous	3,117
essv16812705	mobile element insertion	SAMN01036834	Sequencing	Read depth and paired-end mapping	Heterozygous	2,761
essv16812706	mobile element insertion	SAMN01761220	Sequencing	Read depth and paired-end mapping	Heterozygous	3,325
essv16812707	mobile element insertion	SAMN01761481	Sequencing	Read depth and paired-end mapping	Heterozygous	2,921
essv16812708	mobile element insertion	SAMN01090971	Sequencing	Read depth and paired-end mapping	Heterozygous	2,750
essv16812709	mobile element insertion	SAMN01090970	Sequencing	Read depth and paired-end mapping	Heterozygous	2,778
essv16812710	mobile element insertion	SAMN01090982	Sequencing	Read depth and paired-end mapping	Heterozygous	2,777
essv16812711	mobile element insertion	SAMN01090983	Sequencing	Read depth and paired-end mapping	Heterozygous	2,841
essv16812712	mobile element insertion	SAMN01090941	Sequencing	Read depth and paired-end mapping	Heterozygous	2,580
essv16812713	mobile element insertion	SAMN01761473	Sequencing	Read depth and paired-end mapping	Heterozygous	2,882
essv16812714	mobile element insertion	SAMN01761489	Sequencing	Read depth and paired-end mapping	Heterozygous	2,862
essv16812715	mobile element insertion	SAMN01761582	Sequencing	Read depth and paired-end mapping	Heterozygous	2,801
essv16812716	mobile element insertion	SAMN00801680	Sequencing	Read depth and paired-end mapping	Heterozygous	2,942
essv16812717	mobile element insertion	SAMN00000921	Sequencing	Read depth and paired-end mapping	Heterozygous	2,750
essv16812718	mobile element insertion	SAMN00000925	Sequencing	Read depth and paired-end mapping	Heterozygous	2,725
essv16812719	mobile element insertion	SAMN00000931	Sequencing	Read depth and paired-end mapping	Heterozygous	2,685
essv16812720	mobile element insertion	SAMN00000434	Sequencing	Read depth and paired-end mapping	Heterozygous	2,684
essv16812721	mobile element insertion	SAMN00001620	Sequencing	Read depth and paired-end mapping	Heterozygous	2,821
essv16812722	mobile element insertion	SAMN00000436	Sequencing	Read depth and paired-end mapping	Heterozygous	2,689
essv16812723	mobile element insertion	SAMN00000442	Sequencing	Read depth and paired-end mapping	Heterozygous	2,272
essv16812724	mobile element insertion	SAMN00000444	Sequencing	Read depth and paired-end mapping	Heterozygous	2,816
essv16812725	mobile element insertion	SAMN00000452	Sequencing	Read depth and paired-end mapping	Heterozygous	2,811
essv16812726	mobile element insertion	SAMN00000501	Sequencing	Read depth and paired-end mapping	Heterozygous	2,567
essv16812727	mobile element insertion	SAMN00000522	Sequencing	Read depth and paired-end mapping	Heterozygous	2,834
essv16812728	mobile element insertion	SAMN00007716	Sequencing	Read depth and paired-end mapping	Heterozygous	2,449

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv16812690	Remapped	Perfect	NC_000023.11:g.131 096760_131096761in s?	GRCh38.p12	First Pass	NC_000023.11	ChrX	131,096,760	131,096,760
essv16812691	Remapped	Perfect	NC_000023.11:g.131 096760_131096761in s?	GRCh38.p12	First Pass	NC_000023.11	ChrX	131,096,760	131,096,760
essv16812692	Remapped	Perfect	NC_000023.11:g.131 096760_131096761in s?	GRCh38.p12	First Pass	NC_000023.11	ChrX	131,096,760	131,096,760
essv16812693	Remapped	Perfect	NC_000023.11:g.131 096760_131096761in s?	GRCh38.p12	First Pass	NC_000023.11	ChrX	131,096,760	131,096,760
essv16812694	Remapped	Perfect	NC_000023.11:g.131 096760_131096761in s?	GRCh38.p12	First Pass	NC_000023.11	ChrX	131,096,760	131,096,760
essv16812695	Remapped	Perfect	NC_000023.11:g.131 096760_131096761in s?	GRCh38.p12	First Pass	NC_000023.11	ChrX	131,096,760	131,096,760
essv16812696	Remapped	Perfect	NC_000023.11:g.131 096760_131096761in s?	GRCh38.p12	First Pass	NC_000023.11	ChrX	131,096,760	131,096,760
essv16812697	Remapped	Perfect	NC_000023.11:g.131 096760_131096761in s?	GRCh38.p12	First Pass	NC_000023.11	ChrX	131,096,760	131,096,760
essv16812698	Remapped	Perfect	NC_000023.11:g.131 096760_131096761in s?	GRCh38.p12	First Pass	NC_000023.11	ChrX	131,096,760	131,096,760
essv16812699	Remapped	Perfect	NC_000023.11:g.131 096760_131096761in s?	GRCh38.p12	First Pass	NC_000023.11	ChrX	131,096,760	131,096,760
essv16812700	Remapped	Perfect	NC_000023.11:g.131 096760_131096761in s?	GRCh38.p12	First Pass	NC_000023.11	ChrX	131,096,760	131,096,760
essv16812701	Remapped	Perfect	NC_000023.11:g.131 096760_131096761in s?	GRCh38.p12	First Pass	NC_000023.11	ChrX	131,096,760	131,096,760
essv16812702	Remapped	Perfect	NC_000023.11:g.131 096760_131096761in s?	GRCh38.p12	First Pass	NC_000023.11	ChrX	131,096,760	131,096,760
essv16812703	Remapped	Perfect	NC_000023.11:g.131 096760_131096761in s?	GRCh38.p12	First Pass	NC_000023.11	ChrX	131,096,760	131,096,760
essv16812704	Remapped	Perfect	NC_000023.11:g.131 096760_131096761in s?	GRCh38.p12	First Pass	NC_000023.11	ChrX	131,096,760	131,096,760
essv16812705	Remapped	Perfect	NC_000023.11:g.131 096760_131096761in s?	GRCh38.p12	First Pass	NC_000023.11	ChrX	131,096,760	131,096,760
essv16812706	Remapped	Perfect	NC_000023.11:g.131 096760_131096761in s?	GRCh38.p12	First Pass	NC_000023.11	ChrX	131,096,760	131,096,760
essv16812707	Remapped	Perfect	NC_000023.11:g.131 096760_131096761in s?	GRCh38.p12	First Pass	NC_000023.11	ChrX	131,096,760	131,096,760
essv16812708	Remapped	Perfect	NC_000023.11:g.131 096760_131096761in s?	GRCh38.p12	First Pass	NC_000023.11	ChrX	131,096,760	131,096,760
essv16812709	Remapped	Perfect	NC_000023.11:g.131 096760_131096761in s?	GRCh38.p12	First Pass	NC_000023.11	ChrX	131,096,760	131,096,760
essv16812710	Remapped	Perfect	NC_000023.11:g.131 096760_131096761in s?	GRCh38.p12	First Pass	NC_000023.11	ChrX	131,096,760	131,096,760
essv16812711	Remapped	Perfect	NC_000023.11:g.131 096760_131096761in s?	GRCh38.p12	First Pass	NC_000023.11	ChrX	131,096,760	131,096,760
essv16812712	Remapped	Perfect	NC_000023.11:g.131 096760_131096761in s?	GRCh38.p12	First Pass	NC_000023.11	ChrX	131,096,760	131,096,760
essv16812713	Remapped	Perfect	NC_000023.11:g.131 096760_131096761in s?	GRCh38.p12	First Pass	NC_000023.11	ChrX	131,096,760	131,096,760
essv16812714	Remapped	Perfect	NC_000023.11:g.131 096760_131096761in s?	GRCh38.p12	First Pass	NC_000023.11	ChrX	131,096,760	131,096,760
essv16812715	Remapped	Perfect	NC_000023.11:g.131 096760_131096761in s?	GRCh38.p12	First Pass	NC_000023.11	ChrX	131,096,760	131,096,760
essv16812716	Remapped	Perfect	NC_000023.11:g.131 096760_131096761in s?	GRCh38.p12	First Pass	NC_000023.11	ChrX	131,096,760	131,096,760
essv16812717	Remapped	Perfect	NC_000023.11:g.131 096760_131096761in s?	GRCh38.p12	First Pass	NC_000023.11	ChrX	131,096,760	131,096,760
essv16812718	Remapped	Perfect	NC_000023.11:g.131 096760_131096761in s?	GRCh38.p12	First Pass	NC_000023.11	ChrX	131,096,760	131,096,760
essv16812719	Remapped	Perfect	NC_000023.11:g.131 096760_131096761in s?	GRCh38.p12	First Pass	NC_000023.11	ChrX	131,096,760	131,096,760
essv16812720	Remapped	Perfect	NC_000023.11:g.131 096760_131096761in s?	GRCh38.p12	First Pass	NC_000023.11	ChrX	131,096,760	131,096,760
essv16812721	Remapped	Perfect	NC_000023.11:g.131 096760_131096761in s?	GRCh38.p12	First Pass	NC_000023.11	ChrX	131,096,760	131,096,760
essv16812722	Remapped	Perfect	NC_000023.11:g.131 096760_131096761in s?	GRCh38.p12	First Pass	NC_000023.11	ChrX	131,096,760	131,096,760
essv16812723	Remapped	Perfect	NC_000023.11:g.131 096760_131096761in s?	GRCh38.p12	First Pass	NC_000023.11	ChrX	131,096,760	131,096,760
essv16812724	Remapped	Perfect	NC_000023.11:g.131 096760_131096761in s?	GRCh38.p12	First Pass	NC_000023.11	ChrX	131,096,760	131,096,760
essv16812725	Remapped	Perfect	NC_000023.11:g.131 096760_131096761in s?	GRCh38.p12	First Pass	NC_000023.11	ChrX	131,096,760	131,096,760
essv16812726	Remapped	Perfect	NC_000023.11:g.131 096760_131096761in s?	GRCh38.p12	First Pass	NC_000023.11	ChrX	131,096,760	131,096,760
essv16812727	Remapped	Perfect	NC_000023.11:g.131 096760_131096761in s?	GRCh38.p12	First Pass	NC_000023.11	ChrX	131,096,760	131,096,760
essv16812728	Remapped	Perfect	NC_000023.11:g.131 096760_131096761in s?	GRCh38.p12	First Pass	NC_000023.11	ChrX	131,096,760	131,096,760
essv16812690	Submitted genomic		NC_000023.10:g.130 230734_130230735in s?	GRCh37 (hg19)		NC_000023.10	ChrX	130,230,734	130,230,734
essv16812691	Submitted genomic		NC_000023.10:g.130 230734_130230735in s?	GRCh37 (hg19)		NC_000023.10	ChrX	130,230,734	130,230,734
essv16812692	Submitted genomic		NC_000023.10:g.130 230734_130230735in s?	GRCh37 (hg19)		NC_000023.10	ChrX	130,230,734	130,230,734
essv16812693	Submitted genomic		NC_000023.10:g.130 230734_130230735in s?	GRCh37 (hg19)		NC_000023.10	ChrX	130,230,734	130,230,734
essv16812694	Submitted genomic		NC_000023.10:g.130 230734_130230735in s?	GRCh37 (hg19)		NC_000023.10	ChrX	130,230,734	130,230,734
essv16812695	Submitted genomic		NC_000023.10:g.130 230734_130230735in s?	GRCh37 (hg19)		NC_000023.10	ChrX	130,230,734	130,230,734
essv16812696	Submitted genomic		NC_000023.10:g.130 230734_130230735in s?	GRCh37 (hg19)		NC_000023.10	ChrX	130,230,734	130,230,734
essv16812697	Submitted genomic		NC_000023.10:g.130 230734_130230735in s?	GRCh37 (hg19)		NC_000023.10	ChrX	130,230,734	130,230,734
essv16812698	Submitted genomic		NC_000023.10:g.130 230734_130230735in s?	GRCh37 (hg19)		NC_000023.10	ChrX	130,230,734	130,230,734
essv16812699	Submitted genomic		NC_000023.10:g.130 230734_130230735in s?	GRCh37 (hg19)		NC_000023.10	ChrX	130,230,734	130,230,734
essv16812700	Submitted genomic		NC_000023.10:g.130 230734_130230735in s?	GRCh37 (hg19)		NC_000023.10	ChrX	130,230,734	130,230,734
essv16812701	Submitted genomic		NC_000023.10:g.130 230734_130230735in s?	GRCh37 (hg19)		NC_000023.10	ChrX	130,230,734	130,230,734
essv16812702	Submitted genomic		NC_000023.10:g.130 230734_130230735in s?	GRCh37 (hg19)		NC_000023.10	ChrX	130,230,734	130,230,734
essv16812703	Submitted genomic		NC_000023.10:g.130 230734_130230735in s?	GRCh37 (hg19)		NC_000023.10	ChrX	130,230,734	130,230,734
essv16812704	Submitted genomic		NC_000023.10:g.130 230734_130230735in s?	GRCh37 (hg19)		NC_000023.10	ChrX	130,230,734	130,230,734
essv16812705	Submitted genomic		NC_000023.10:g.130 230734_130230735in s?	GRCh37 (hg19)		NC_000023.10	ChrX	130,230,734	130,230,734
essv16812706	Submitted genomic		NC_000023.10:g.130 230734_130230735in s?	GRCh37 (hg19)		NC_000023.10	ChrX	130,230,734	130,230,734
essv16812707	Submitted genomic		NC_000023.10:g.130 230734_130230735in s?	GRCh37 (hg19)		NC_000023.10	ChrX	130,230,734	130,230,734
essv16812708	Submitted genomic		NC_000023.10:g.130 230734_130230735in s?	GRCh37 (hg19)		NC_000023.10	ChrX	130,230,734	130,230,734
essv16812709	Submitted genomic		NC_000023.10:g.130 230734_130230735in s?	GRCh37 (hg19)		NC_000023.10	ChrX	130,230,734	130,230,734
essv16812710	Submitted genomic		NC_000023.10:g.130 230734_130230735in s?	GRCh37 (hg19)		NC_000023.10	ChrX	130,230,734	130,230,734
essv16812711	Submitted genomic		NC_000023.10:g.130 230734_130230735in s?	GRCh37 (hg19)		NC_000023.10	ChrX	130,230,734	130,230,734
essv16812712	Submitted genomic		NC_000023.10:g.130 230734_130230735in s?	GRCh37 (hg19)		NC_000023.10	ChrX	130,230,734	130,230,734
essv16812713	Submitted genomic		NC_000023.10:g.130 230734_130230735in s?	GRCh37 (hg19)		NC_000023.10	ChrX	130,230,734	130,230,734
essv16812714	Submitted genomic		NC_000023.10:g.130 230734_130230735in s?	GRCh37 (hg19)		NC_000023.10	ChrX	130,230,734	130,230,734
essv16812715	Submitted genomic		NC_000023.10:g.130 230734_130230735in s?	GRCh37 (hg19)		NC_000023.10	ChrX	130,230,734	130,230,734
essv16812716	Submitted genomic		NC_000023.10:g.130 230734_130230735in s?	GRCh37 (hg19)		NC_000023.10	ChrX	130,230,734	130,230,734
essv16812717	Submitted genomic		NC_000023.10:g.130 230734_130230735in s?	GRCh37 (hg19)		NC_000023.10	ChrX	130,230,734	130,230,734
essv16812718	Submitted genomic		NC_000023.10:g.130 230734_130230735in s?	GRCh37 (hg19)		NC_000023.10	ChrX	130,230,734	130,230,734
essv16812719	Submitted genomic		NC_000023.10:g.130 230734_130230735in s?	GRCh37 (hg19)		NC_000023.10	ChrX	130,230,734	130,230,734
essv16812720	Submitted genomic		NC_000023.10:g.130 230734_130230735in s?	GRCh37 (hg19)		NC_000023.10	ChrX	130,230,734	130,230,734
essv16812721	Submitted genomic		NC_000023.10:g.130 230734_130230735in s?	GRCh37 (hg19)		NC_000023.10	ChrX	130,230,734	130,230,734
essv16812722	Submitted genomic		NC_000023.10:g.130 230734_130230735in s?	GRCh37 (hg19)		NC_000023.10	ChrX	130,230,734	130,230,734
essv16812723	Submitted genomic		NC_000023.10:g.130 230734_130230735in s?	GRCh37 (hg19)		NC_000023.10	ChrX	130,230,734	130,230,734
essv16812724	Submitted genomic		NC_000023.10:g.130 230734_130230735in s?	GRCh37 (hg19)		NC_000023.10	ChrX	130,230,734	130,230,734
essv16812725	Submitted genomic		NC_000023.10:g.130 230734_130230735in s?	GRCh37 (hg19)		NC_000023.10	ChrX	130,230,734	130,230,734
essv16812726	Submitted genomic		NC_000023.10:g.130 230734_130230735in s?	GRCh37 (hg19)		NC_000023.10	ChrX	130,230,734	130,230,734
essv16812727	Submitted genomic		NC_000023.10:g.130 230734_130230735in s?	GRCh37 (hg19)		NC_000023.10	ChrX	130,230,734	130,230,734
essv16812728	Submitted genomic		NC_000023.10:g.130 230734_130230735in s?	GRCh37 (hg19)		NC_000023.10	ChrX	130,230,734	130,230,734

dbVar

Database of genomic structural variation

esv3817087

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.