esv3647976

Organism: Homo sapiens

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

Variant Calls:67
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: 299 SVs from 29 studies. See in: genome view

Remapped(Score: Perfect):47,195,960-47,195,960

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3647976	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
esv3647976	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000022.10	Chr22	47,591,710	47,591,710

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
essv16445888	alu insertion	SAMN00009123	Sequencing	Read depth and paired-end mapping	Heterozygous	2,733
essv16445889	alu insertion	SAMN00009178	Sequencing	Read depth and paired-end mapping	Heterozygous	2,703
essv16445890	alu insertion	SAMN00009242	Sequencing	Read depth and paired-end mapping	Heterozygous	2,581
essv16445891	alu insertion	SAMN00009254	Sequencing	Read depth and paired-end mapping	Heterozygous	2,508
essv16445892	alu insertion	SAMN00014344	Sequencing	Read depth and paired-end mapping	Heterozygous	2,999
essv16445893	alu insertion	SAMN00014350	Sequencing	Read depth and paired-end mapping	Heterozygous	2,736
essv16445894	alu insertion	SAMN00630195	Sequencing	Read depth and paired-end mapping	Heterozygous	3,101
essv16445895	alu insertion	SAMN00262968	Sequencing	Read depth and paired-end mapping	Heterozygous	3,187
essv16445896	alu insertion	SAMN00249703	Sequencing	Read depth and paired-end mapping	Heterozygous	2,640
essv16445897	alu insertion	SAMN01091055	Sequencing	Read depth and paired-end mapping	Heterozygous	3,351
essv16445898	alu insertion	SAMN01761368	Sequencing	Read depth and paired-end mapping	Heterozygous	2,813
essv16445899	alu insertion	SAMN01761370	Sequencing	Read depth and paired-end mapping	Heterozygous	2,736
essv16445900	alu insertion	SAMN00780014	Sequencing	Read depth and paired-end mapping	Heterozygous	2,864
essv16445901	alu insertion	SAMN01036825	Sequencing	Read depth and paired-end mapping	Heterozygous	2,879
essv16445902	alu insertion	SAMN00780017	Sequencing	Read depth and paired-end mapping	Heterozygous	2,758
essv16445903	alu insertion	SAMN01036836	Sequencing	Read depth and paired-end mapping	Heterozygous	2,831
essv16445904	alu insertion	SAMN01036769	Sequencing	Read depth and paired-end mapping	Homozygous	2,858
essv16445905	alu insertion	SAMN01036770	Sequencing	Read depth and paired-end mapping	Heterozygous	2,914
essv16445906	alu insertion	SAMN01096687	Sequencing	Read depth and paired-end mapping	Heterozygous	2,738
essv16445907	alu insertion	SAMN01090874	Sequencing	Read depth and paired-end mapping	Heterozygous	3,163
essv16445908	alu insertion	SAMN01036815	Sequencing	Read depth and paired-end mapping	Heterozygous	3,205
essv16445909	alu insertion	SAMN01036819	Sequencing	Read depth and paired-end mapping	Heterozygous	3,300
essv16445910	alu insertion	SAMN01036821	Sequencing	Read depth and paired-end mapping	Heterozygous	3,308
essv16445911	alu insertion	SAMN01761295	Sequencing	Read depth and paired-end mapping	Heterozygous	3,217
essv16445912	alu insertion	SAMN01761312	Sequencing	Read depth and paired-end mapping	Heterozygous	3,328
essv16445913	alu insertion	SAMN01090897	Sequencing	Read depth and paired-end mapping	Heterozygous	2,876
essv16445914	alu insertion	SAMN01096700	Sequencing	Read depth and paired-end mapping	Heterozygous	2,746
essv16445915	alu insertion	SAMN01090971	Sequencing	Read depth and paired-end mapping	Heterozygous	2,750
essv16445916	alu insertion	SAMN01090969	Sequencing	Read depth and paired-end mapping	Heterozygous	2,890
essv16445917	alu insertion	SAMN01090968	Sequencing	Read depth and paired-end mapping	Heterozygous	2,781
essv16445918	alu insertion	SAMN01096776	Sequencing	Read depth and paired-end mapping	Heterozygous	2,633
essv16445919	alu insertion	SAMN01090990	Sequencing	Read depth and paired-end mapping	Heterozygous	2,766
essv16445920	alu insertion	SAMN01096783	Sequencing	Read depth and paired-end mapping	Heterozygous	2,691
essv16445921	alu insertion	SAMN01090941	Sequencing	Read depth and paired-end mapping	Heterozygous	2,580
essv16445922	alu insertion	SAMN01096685	Sequencing	Read depth and paired-end mapping	Heterozygous	2,673
essv16445923	alu insertion	SAMN01090994	Sequencing	Read depth and paired-end mapping	Heterozygous	2,826
essv16445924	alu insertion	SAMN01096751	Sequencing	Read depth and paired-end mapping	Heterozygous	2,759
essv16445925	alu insertion	SAMN01096717	Sequencing	Read depth and paired-end mapping	Heterozygous	2,533
essv16445926	alu insertion	SAMN01091029	Sequencing	Read depth and paired-end mapping	Heterozygous	2,716
essv16445927	alu insertion	SAMN01096791	Sequencing	Read depth and paired-end mapping	Heterozygous	2,614
essv16445928	alu insertion	SAMN01090998	Sequencing	Read depth and paired-end mapping	Heterozygous	2,627
essv16445929	alu insertion	SAMN01096699	Sequencing	Read depth and paired-end mapping	Heterozygous	2,645
essv16445930	alu insertion	SAMN01096795	Sequencing	Read depth and paired-end mapping	Heterozygous	2,562
essv16445931	alu insertion	SAMN01091040	Sequencing	Read depth and paired-end mapping	Heterozygous	2,633
essv16445932	alu insertion	SAMN01761566	Sequencing	Read depth and paired-end mapping	Heterozygous	2,183
essv16445933	alu insertion	SAMN01096806	Sequencing	Read depth and paired-end mapping	Heterozygous	2,544
essv16445934	alu insertion	SAMN01090965	Sequencing	Read depth and paired-end mapping	Heterozygous	2,665
essv16445935	alu insertion	SAMN01090966	Sequencing	Read depth and paired-end mapping	Heterozygous	2,613
essv16445936	alu insertion	SAMN00000425	Sequencing	Read depth and paired-end mapping	Heterozygous	2,630
essv16445937	alu insertion	SAMN00001625	Sequencing	Read depth and paired-end mapping	Heterozygous	3,281
essv16445938	alu insertion	SAMN00001021	Sequencing	Read depth and paired-end mapping	Heterozygous	3,301
essv16445939	alu insertion	SAMN00000479	Sequencing	Read depth and paired-end mapping	Heterozygous	3,240
essv16445940	alu insertion	SAMN00000547	Sequencing	Read depth and paired-end mapping	Heterozygous	3,222
essv16445941	alu insertion	SAMN00001674	Sequencing	Read depth and paired-end mapping	Heterozygous	3,102
essv16445942	alu insertion	SAMN00004467	Sequencing	Read depth and paired-end mapping	Heterozygous	2,546
essv16445943	alu insertion	SAMN00007821	Sequencing	Read depth and paired-end mapping	Heterozygous	3,467
essv16445944	alu insertion	SAMN00007880	Sequencing	Read depth and paired-end mapping	Heterozygous	2,940
essv16445945	alu insertion	SAMN00007884	Sequencing	Read depth and paired-end mapping	Heterozygous	2,873
essv16445946	alu insertion	SAMN00007888	Sequencing	Read depth and paired-end mapping	Heterozygous	2,782
essv16445947	alu insertion	SAMN00007892	Sequencing	Read depth and paired-end mapping	Heterozygous	2,830
essv16445948	alu insertion	SAMN00007937	Sequencing	Read depth and paired-end mapping	Heterozygous	2,756
essv16445949	alu insertion	SAMN00007950	Sequencing	Read depth and paired-end mapping	Homozygous	2,674
essv16445950	alu insertion	SAMN00007951	Sequencing	Read depth and paired-end mapping	Heterozygous	2,651
essv16445951	alu insertion	SAMN00007961	Sequencing	Read depth and paired-end mapping	Heterozygous	2,652
essv16445952	alu insertion	SAMN00007964	Sequencing	Read depth and paired-end mapping	Heterozygous	2,597
essv16445953	alu insertion	SAMN00004497	Sequencing	Read depth and paired-end mapping	Heterozygous	2,798
essv16445954	alu insertion	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
essv16445888	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445889	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445890	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445891	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445892	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445893	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445894	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445895	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445896	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445897	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445898	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445899	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445900	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445901	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445902	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445903	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445904	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445905	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445906	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445907	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445908	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445909	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445910	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445911	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445912	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445913	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445914	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445915	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445916	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445917	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445918	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445919	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445920	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445921	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445922	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445923	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445924	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445925	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445926	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445927	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445928	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445929	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445930	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445931	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445932	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445933	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445934	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445935	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445936	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445937	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445938	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445939	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445940	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445941	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445942	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445943	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445944	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445945	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445946	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445947	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445948	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445949	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445950	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445951	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445952	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445953	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445954	Remapped	Perfect	NC_000022.11:g.471 95960_47195961ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	47,195,960	47,195,960
essv16445888	Submitted genomic		NC_000022.10:g.475 91710_47591711ins?	GRCh37 (hg19)		NC_000022.10	Chr22	47,591,710	47,591,710
essv16445889	Submitted genomic		NC_000022.10:g.475 91710_47591711ins?	GRCh37 (hg19)		NC_000022.10	Chr22	47,591,710	47,591,710
essv16445890	Submitted genomic		NC_000022.10:g.475 91710_47591711ins?	GRCh37 (hg19)		NC_000022.10	Chr22	47,591,710	47,591,710
essv16445891	Submitted genomic		NC_000022.10:g.475 91710_47591711ins?	GRCh37 (hg19)		NC_000022.10	Chr22	47,591,710	47,591,710
essv16445892	Submitted genomic		NC_000022.10:g.475 91710_47591711ins?	GRCh37 (hg19)		NC_000022.10	Chr22	47,591,710	47,591,710
essv16445893	Submitted genomic		NC_000022.10:g.475 91710_47591711ins?	GRCh37 (hg19)		NC_000022.10	Chr22	47,591,710	47,591,710
essv16445894	Submitted genomic		NC_000022.10:g.475 91710_47591711ins?	GRCh37 (hg19)		NC_000022.10	Chr22	47,591,710	47,591,710
essv16445895	Submitted genomic		NC_000022.10:g.475 91710_47591711ins?	GRCh37 (hg19)		NC_000022.10	Chr22	47,591,710	47,591,710
essv16445896	Submitted genomic		NC_000022.10:g.475 91710_47591711ins?	GRCh37 (hg19)		NC_000022.10	Chr22	47,591,710	47,591,710
essv16445897	Submitted genomic		NC_000022.10:g.475 91710_47591711ins?	GRCh37 (hg19)		NC_000022.10	Chr22	47,591,710	47,591,710
essv16445898	Submitted genomic		NC_000022.10:g.475 91710_47591711ins?	GRCh37 (hg19)		NC_000022.10	Chr22	47,591,710	47,591,710
essv16445899	Submitted genomic		NC_000022.10:g.475 91710_47591711ins?	GRCh37 (hg19)		NC_000022.10	Chr22	47,591,710	47,591,710
essv16445900	Submitted genomic		NC_000022.10:g.475 91710_47591711ins?	GRCh37 (hg19)		NC_000022.10	Chr22	47,591,710	47,591,710
essv16445901	Submitted genomic		NC_000022.10:g.475 91710_47591711ins?	GRCh37 (hg19)		NC_000022.10	Chr22	47,591,710	47,591,710
essv16445902	Submitted genomic		NC_000022.10:g.475 91710_47591711ins?	GRCh37 (hg19)		NC_000022.10	Chr22	47,591,710	47,591,710
essv16445903	Submitted genomic		NC_000022.10:g.475 91710_47591711ins?	GRCh37 (hg19)		NC_000022.10	Chr22	47,591,710	47,591,710
essv16445904	Submitted genomic		NC_000022.10:g.475 91710_47591711ins?	GRCh37 (hg19)		NC_000022.10	Chr22	47,591,710	47,591,710
essv16445905	Submitted genomic		NC_000022.10:g.475 91710_47591711ins?	GRCh37 (hg19)		NC_000022.10	Chr22	47,591,710	47,591,710
essv16445906	Submitted genomic		NC_000022.10:g.475 91710_47591711ins?	GRCh37 (hg19)		NC_000022.10	Chr22	47,591,710	47,591,710
essv16445907	Submitted genomic		NC_000022.10:g.475 91710_47591711ins?	GRCh37 (hg19)		NC_000022.10	Chr22	47,591,710	47,591,710
essv16445908	Submitted genomic		NC_000022.10:g.475 91710_47591711ins?	GRCh37 (hg19)		NC_000022.10	Chr22	47,591,710	47,591,710
essv16445909	Submitted genomic		NC_000022.10:g.475 91710_47591711ins?	GRCh37 (hg19)		NC_000022.10	Chr22	47,591,710	47,591,710
essv16445910	Submitted genomic		NC_000022.10:g.475 91710_47591711ins?	GRCh37 (hg19)		NC_000022.10	Chr22	47,591,710	47,591,710
essv16445911	Submitted genomic		NC_000022.10:g.475 91710_47591711ins?	GRCh37 (hg19)		NC_000022.10	Chr22	47,591,710	47,591,710
essv16445912	Submitted genomic		NC_000022.10:g.475 91710_47591711ins?	GRCh37 (hg19)		NC_000022.10	Chr22	47,591,710	47,591,710
essv16445913	Submitted genomic		NC_000022.10:g.475 91710_47591711ins?	GRCh37 (hg19)		NC_000022.10	Chr22	47,591,710	47,591,710
essv16445914	Submitted genomic		NC_000022.10:g.475 91710_47591711ins?	GRCh37 (hg19)		NC_000022.10	Chr22	47,591,710	47,591,710
essv16445915	Submitted genomic		NC_000022.10:g.475 91710_47591711ins?	GRCh37 (hg19)		NC_000022.10	Chr22	47,591,710	47,591,710
essv16445916	Submitted genomic		NC_000022.10:g.475 91710_47591711ins?	GRCh37 (hg19)		NC_000022.10	Chr22	47,591,710	47,591,710
essv16445917	Submitted genomic		NC_000022.10:g.475 91710_47591711ins?	GRCh37 (hg19)		NC_000022.10	Chr22	47,591,710	47,591,710
essv16445918	Submitted genomic		NC_000022.10:g.475 91710_47591711ins?	GRCh37 (hg19)		NC_000022.10	Chr22	47,591,710	47,591,710
essv16445919	Submitted genomic		NC_000022.10:g.475 91710_47591711ins?	GRCh37 (hg19)		NC_000022.10	Chr22	47,591,710	47,591,710
essv16445920	Submitted genomic		NC_000022.10:g.475 91710_47591711ins?	GRCh37 (hg19)		NC_000022.10	Chr22	47,591,710	47,591,710

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dbVar

Database of genomic structural variation

esv3647976

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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.