esv3647941

Organism: Homo sapiens

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

Variant Calls:51
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: 320 SVs from 32 studies. See in: genome view

Remapped(Score: Perfect):46,105,406-46,105,406

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3647941	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000022.11	Chr22	46,105,406	46,105,406
esv3647941	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000022.10	Chr22	46,501,286	46,501,286

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
essv16444880	alu insertion	SAMN00006583	Sequencing	Read depth and paired-end mapping	Heterozygous	2,480
essv16444881	alu insertion	SAMN00006586	Sequencing	Read depth and paired-end mapping	Heterozygous	2,626
essv16444882	alu insertion	SAMN00255125	Sequencing	Read depth and paired-end mapping	Heterozygous	3,547
essv16444883	alu insertion	SAMN00249724	Sequencing	Read depth and paired-end mapping	Heterozygous	2,551
essv16444884	alu insertion	SAMN00262974	Sequencing	Read depth and paired-end mapping	Heterozygous	3,255
essv16444885	alu insertion	SAMN00262977	Sequencing	Read depth and paired-end mapping	Heterozygous	3,257
essv16444886	alu insertion	SAMN01091056	Sequencing	Read depth and paired-end mapping	Heterozygous	3,207
essv16444887	alu insertion	SAMN01761208	Sequencing	Read depth and paired-end mapping	Heterozygous	3,316
essv16444888	alu insertion	SAMN01761229	Sequencing	Read depth and paired-end mapping	Heterozygous	3,411
essv16444889	alu insertion	SAMN01090798	Sequencing	Read depth and paired-end mapping	Heterozygous	3,064
essv16444890	alu insertion	SAMN01761239	Sequencing	Read depth and paired-end mapping	Heterozygous	3,286
essv16444891	alu insertion	SAMN01761243	Sequencing	Read depth and paired-end mapping	Heterozygous	3,270
essv16444892	alu insertion	SAMN01036785	Sequencing	Read depth and paired-end mapping	Heterozygous	3,177
essv16444893	alu insertion	SAMN01036809	Sequencing	Read depth and paired-end mapping	Heterozygous	3,100
essv16444894	alu insertion	SAMN01090883	Sequencing	Read depth and paired-end mapping	Heterozygous	3,017
essv16444895	alu insertion	SAMN01761302	Sequencing	Read depth and paired-end mapping	Heterozygous	3,284
essv16444896	alu insertion	SAMN01761310	Sequencing	Read depth and paired-end mapping	Heterozygous	3,227
essv16444897	alu insertion	SAMN01090892	Sequencing	Read depth and paired-end mapping	Heterozygous	2,959
essv16444898	alu insertion	SAMN01090774	Sequencing	Read depth and paired-end mapping	Heterozygous	3,029
essv16444899	alu insertion	SAMN01090752	Sequencing	Read depth and paired-end mapping	Heterozygous	3,116
essv16444900	alu insertion	SAMN01090754	Sequencing	Read depth and paired-end mapping	Heterozygous	2,921
essv16444901	alu insertion	SAMN01090755	Sequencing	Read depth and paired-end mapping	Heterozygous	2,881
essv16444902	alu insertion	SAMN01090844	Sequencing	Read depth and paired-end mapping	Heterozygous	2,911
essv16444903	alu insertion	SAMN01090897	Sequencing	Read depth and paired-end mapping	Heterozygous	2,876
essv16444904	alu insertion	SAMN01036789	Sequencing	Read depth and paired-end mapping	Heterozygous	3,228
essv16444905	alu insertion	SAMN01036793	Sequencing	Read depth and paired-end mapping	Heterozygous	3,204
essv16444906	alu insertion	SAMN01090794	Sequencing	Read depth and paired-end mapping	Heterozygous	3,067
essv16444907	alu insertion	SAMN01090758	Sequencing	Read depth and paired-end mapping	Heterozygous	3,041
essv16444908	alu insertion	SAMN00001582	Sequencing	Read depth and paired-end mapping	Heterozygous	3,046
essv16444909	alu insertion	SAMN00001590	Sequencing	Read depth and paired-end mapping	Heterozygous	3,076
essv16444910	alu insertion	SAMN00001627	Sequencing	Read depth and paired-end mapping	Heterozygous	3,105
essv16444911	alu insertion	SAMN00000482	Sequencing	Read depth and paired-end mapping	Heterozygous	2,317
essv16444912	alu insertion	SAMN00001044	Sequencing	Read depth and paired-end mapping	Heterozygous	3,190
essv16444913	alu insertion	SAMN00001055	Sequencing	Read depth and paired-end mapping	Heterozygous	2,911
essv16444914	alu insertion	SAMN00000547	Sequencing	Read depth and paired-end mapping	Heterozygous	3,222
essv16444915	alu insertion	SAMN00001685	Sequencing	Read depth and paired-end mapping	Heterozygous	3,296
essv16444916	alu insertion	SAMN00001339	Sequencing	Read depth and paired-end mapping	Heterozygous	3,222
essv16444917	alu insertion	SAMN00001104	Sequencing	Read depth and paired-end mapping	Heterozygous	2,712
essv16444918	alu insertion	SAMN00001115	Sequencing	Read depth and paired-end mapping	Homozygous	2,431
essv16444919	alu insertion	SAMN00001117	Sequencing	Read depth and paired-end mapping	Heterozygous	4,071
essv16444920	alu insertion	SAMN00001152	Sequencing	Read depth and paired-end mapping	Heterozygous	3,097
essv16444921	alu insertion	SAMN00001183	Sequencing	Read depth and paired-end mapping	Heterozygous	2,986
essv16444922	alu insertion	SAMN00001188	Sequencing	Read depth and paired-end mapping	Heterozygous	2,659
essv16444923	alu insertion	SAMN00001195	Sequencing	Read depth and paired-end mapping	Heterozygous	3,410
essv16444924	alu insertion	SAMN00007735	Sequencing	Read depth and paired-end mapping	Heterozygous	3,097
essv16444925	alu insertion	SAMN00007810	Sequencing	Read depth and paired-end mapping	Heterozygous	3,058
essv16444926	alu insertion	SAMN00007839	Sequencing	Read depth and paired-end mapping	Heterozygous	2,433
essv16444927	alu insertion	SAMN00006625	Sequencing	Read depth and paired-end mapping	Heterozygous	3,228
essv16444928	alu insertion	SAMN00006626	Sequencing	Read depth and paired-end mapping	Heterozygous	3,149
essv16444929	alu insertion	SAMN00007856	Sequencing	Read depth and paired-end mapping	Heterozygous	2,397
essv16444930	alu insertion	SAMN00006629	Sequencing	Read depth and paired-end mapping	Heterozygous	3,232

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv16444880	Remapped	Perfect	NC_000022.11:g.461 05406_46105407ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	46,105,406	46,105,406
essv16444881	Remapped	Perfect	NC_000022.11:g.461 05406_46105407ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	46,105,406	46,105,406
essv16444882	Remapped	Perfect	NC_000022.11:g.461 05406_46105407ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	46,105,406	46,105,406
essv16444883	Remapped	Perfect	NC_000022.11:g.461 05406_46105407ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	46,105,406	46,105,406
essv16444884	Remapped	Perfect	NC_000022.11:g.461 05406_46105407ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	46,105,406	46,105,406
essv16444885	Remapped	Perfect	NC_000022.11:g.461 05406_46105407ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	46,105,406	46,105,406
essv16444886	Remapped	Perfect	NC_000022.11:g.461 05406_46105407ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	46,105,406	46,105,406
essv16444887	Remapped	Perfect	NC_000022.11:g.461 05406_46105407ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	46,105,406	46,105,406
essv16444888	Remapped	Perfect	NC_000022.11:g.461 05406_46105407ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	46,105,406	46,105,406
essv16444889	Remapped	Perfect	NC_000022.11:g.461 05406_46105407ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	46,105,406	46,105,406
essv16444890	Remapped	Perfect	NC_000022.11:g.461 05406_46105407ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	46,105,406	46,105,406
essv16444891	Remapped	Perfect	NC_000022.11:g.461 05406_46105407ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	46,105,406	46,105,406
essv16444892	Remapped	Perfect	NC_000022.11:g.461 05406_46105407ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	46,105,406	46,105,406
essv16444893	Remapped	Perfect	NC_000022.11:g.461 05406_46105407ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	46,105,406	46,105,406
essv16444894	Remapped	Perfect	NC_000022.11:g.461 05406_46105407ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	46,105,406	46,105,406
essv16444895	Remapped	Perfect	NC_000022.11:g.461 05406_46105407ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	46,105,406	46,105,406
essv16444896	Remapped	Perfect	NC_000022.11:g.461 05406_46105407ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	46,105,406	46,105,406
essv16444897	Remapped	Perfect	NC_000022.11:g.461 05406_46105407ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	46,105,406	46,105,406
essv16444898	Remapped	Perfect	NC_000022.11:g.461 05406_46105407ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	46,105,406	46,105,406
essv16444899	Remapped	Perfect	NC_000022.11:g.461 05406_46105407ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	46,105,406	46,105,406
essv16444900	Remapped	Perfect	NC_000022.11:g.461 05406_46105407ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	46,105,406	46,105,406
essv16444901	Remapped	Perfect	NC_000022.11:g.461 05406_46105407ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	46,105,406	46,105,406
essv16444902	Remapped	Perfect	NC_000022.11:g.461 05406_46105407ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	46,105,406	46,105,406
essv16444903	Remapped	Perfect	NC_000022.11:g.461 05406_46105407ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	46,105,406	46,105,406
essv16444904	Remapped	Perfect	NC_000022.11:g.461 05406_46105407ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	46,105,406	46,105,406
essv16444905	Remapped	Perfect	NC_000022.11:g.461 05406_46105407ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	46,105,406	46,105,406
essv16444906	Remapped	Perfect	NC_000022.11:g.461 05406_46105407ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	46,105,406	46,105,406
essv16444907	Remapped	Perfect	NC_000022.11:g.461 05406_46105407ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	46,105,406	46,105,406
essv16444908	Remapped	Perfect	NC_000022.11:g.461 05406_46105407ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	46,105,406	46,105,406
essv16444909	Remapped	Perfect	NC_000022.11:g.461 05406_46105407ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	46,105,406	46,105,406
essv16444910	Remapped	Perfect	NC_000022.11:g.461 05406_46105407ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	46,105,406	46,105,406
essv16444911	Remapped	Perfect	NC_000022.11:g.461 05406_46105407ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	46,105,406	46,105,406
essv16444912	Remapped	Perfect	NC_000022.11:g.461 05406_46105407ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	46,105,406	46,105,406
essv16444913	Remapped	Perfect	NC_000022.11:g.461 05406_46105407ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	46,105,406	46,105,406
essv16444914	Remapped	Perfect	NC_000022.11:g.461 05406_46105407ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	46,105,406	46,105,406
essv16444915	Remapped	Perfect	NC_000022.11:g.461 05406_46105407ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	46,105,406	46,105,406
essv16444916	Remapped	Perfect	NC_000022.11:g.461 05406_46105407ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	46,105,406	46,105,406
essv16444917	Remapped	Perfect	NC_000022.11:g.461 05406_46105407ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	46,105,406	46,105,406
essv16444918	Remapped	Perfect	NC_000022.11:g.461 05406_46105407ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	46,105,406	46,105,406
essv16444919	Remapped	Perfect	NC_000022.11:g.461 05406_46105407ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	46,105,406	46,105,406
essv16444920	Remapped	Perfect	NC_000022.11:g.461 05406_46105407ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	46,105,406	46,105,406
essv16444921	Remapped	Perfect	NC_000022.11:g.461 05406_46105407ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	46,105,406	46,105,406
essv16444922	Remapped	Perfect	NC_000022.11:g.461 05406_46105407ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	46,105,406	46,105,406
essv16444923	Remapped	Perfect	NC_000022.11:g.461 05406_46105407ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	46,105,406	46,105,406
essv16444924	Remapped	Perfect	NC_000022.11:g.461 05406_46105407ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	46,105,406	46,105,406
essv16444925	Remapped	Perfect	NC_000022.11:g.461 05406_46105407ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	46,105,406	46,105,406
essv16444926	Remapped	Perfect	NC_000022.11:g.461 05406_46105407ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	46,105,406	46,105,406
essv16444927	Remapped	Perfect	NC_000022.11:g.461 05406_46105407ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	46,105,406	46,105,406
essv16444928	Remapped	Perfect	NC_000022.11:g.461 05406_46105407ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	46,105,406	46,105,406
essv16444929	Remapped	Perfect	NC_000022.11:g.461 05406_46105407ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	46,105,406	46,105,406
essv16444930	Remapped	Perfect	NC_000022.11:g.461 05406_46105407ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	46,105,406	46,105,406
essv16444880	Submitted genomic		NC_000022.10:g.465 01286_46501287ins?	GRCh37 (hg19)		NC_000022.10	Chr22	46,501,286	46,501,286
essv16444881	Submitted genomic		NC_000022.10:g.465 01286_46501287ins?	GRCh37 (hg19)		NC_000022.10	Chr22	46,501,286	46,501,286
essv16444882	Submitted genomic		NC_000022.10:g.465 01286_46501287ins?	GRCh37 (hg19)		NC_000022.10	Chr22	46,501,286	46,501,286
essv16444883	Submitted genomic		NC_000022.10:g.465 01286_46501287ins?	GRCh37 (hg19)		NC_000022.10	Chr22	46,501,286	46,501,286
essv16444884	Submitted genomic		NC_000022.10:g.465 01286_46501287ins?	GRCh37 (hg19)		NC_000022.10	Chr22	46,501,286	46,501,286
essv16444885	Submitted genomic		NC_000022.10:g.465 01286_46501287ins?	GRCh37 (hg19)		NC_000022.10	Chr22	46,501,286	46,501,286
essv16444886	Submitted genomic		NC_000022.10:g.465 01286_46501287ins?	GRCh37 (hg19)		NC_000022.10	Chr22	46,501,286	46,501,286
essv16444887	Submitted genomic		NC_000022.10:g.465 01286_46501287ins?	GRCh37 (hg19)		NC_000022.10	Chr22	46,501,286	46,501,286
essv16444888	Submitted genomic		NC_000022.10:g.465 01286_46501287ins?	GRCh37 (hg19)		NC_000022.10	Chr22	46,501,286	46,501,286
essv16444889	Submitted genomic		NC_000022.10:g.465 01286_46501287ins?	GRCh37 (hg19)		NC_000022.10	Chr22	46,501,286	46,501,286
essv16444890	Submitted genomic		NC_000022.10:g.465 01286_46501287ins?	GRCh37 (hg19)		NC_000022.10	Chr22	46,501,286	46,501,286
essv16444891	Submitted genomic		NC_000022.10:g.465 01286_46501287ins?	GRCh37 (hg19)		NC_000022.10	Chr22	46,501,286	46,501,286
essv16444892	Submitted genomic		NC_000022.10:g.465 01286_46501287ins?	GRCh37 (hg19)		NC_000022.10	Chr22	46,501,286	46,501,286
essv16444893	Submitted genomic		NC_000022.10:g.465 01286_46501287ins?	GRCh37 (hg19)		NC_000022.10	Chr22	46,501,286	46,501,286
essv16444894	Submitted genomic		NC_000022.10:g.465 01286_46501287ins?	GRCh37 (hg19)		NC_000022.10	Chr22	46,501,286	46,501,286
essv16444895	Submitted genomic		NC_000022.10:g.465 01286_46501287ins?	GRCh37 (hg19)		NC_000022.10	Chr22	46,501,286	46,501,286
essv16444896	Submitted genomic		NC_000022.10:g.465 01286_46501287ins?	GRCh37 (hg19)		NC_000022.10	Chr22	46,501,286	46,501,286
essv16444897	Submitted genomic		NC_000022.10:g.465 01286_46501287ins?	GRCh37 (hg19)		NC_000022.10	Chr22	46,501,286	46,501,286
essv16444898	Submitted genomic		NC_000022.10:g.465 01286_46501287ins?	GRCh37 (hg19)		NC_000022.10	Chr22	46,501,286	46,501,286
essv16444899	Submitted genomic		NC_000022.10:g.465 01286_46501287ins?	GRCh37 (hg19)		NC_000022.10	Chr22	46,501,286	46,501,286
essv16444900	Submitted genomic		NC_000022.10:g.465 01286_46501287ins?	GRCh37 (hg19)		NC_000022.10	Chr22	46,501,286	46,501,286
essv16444901	Submitted genomic		NC_000022.10:g.465 01286_46501287ins?	GRCh37 (hg19)		NC_000022.10	Chr22	46,501,286	46,501,286
essv16444902	Submitted genomic		NC_000022.10:g.465 01286_46501287ins?	GRCh37 (hg19)		NC_000022.10	Chr22	46,501,286	46,501,286
essv16444903	Submitted genomic		NC_000022.10:g.465 01286_46501287ins?	GRCh37 (hg19)		NC_000022.10	Chr22	46,501,286	46,501,286
essv16444904	Submitted genomic		NC_000022.10:g.465 01286_46501287ins?	GRCh37 (hg19)		NC_000022.10	Chr22	46,501,286	46,501,286
essv16444905	Submitted genomic		NC_000022.10:g.465 01286_46501287ins?	GRCh37 (hg19)		NC_000022.10	Chr22	46,501,286	46,501,286
essv16444906	Submitted genomic		NC_000022.10:g.465 01286_46501287ins?	GRCh37 (hg19)		NC_000022.10	Chr22	46,501,286	46,501,286
essv16444907	Submitted genomic		NC_000022.10:g.465 01286_46501287ins?	GRCh37 (hg19)		NC_000022.10	Chr22	46,501,286	46,501,286
essv16444908	Submitted genomic		NC_000022.10:g.465 01286_46501287ins?	GRCh37 (hg19)		NC_000022.10	Chr22	46,501,286	46,501,286
essv16444909	Submitted genomic		NC_000022.10:g.465 01286_46501287ins?	GRCh37 (hg19)		NC_000022.10	Chr22	46,501,286	46,501,286
essv16444910	Submitted genomic		NC_000022.10:g.465 01286_46501287ins?	GRCh37 (hg19)		NC_000022.10	Chr22	46,501,286	46,501,286
essv16444911	Submitted genomic		NC_000022.10:g.465 01286_46501287ins?	GRCh37 (hg19)		NC_000022.10	Chr22	46,501,286	46,501,286
essv16444912	Submitted genomic		NC_000022.10:g.465 01286_46501287ins?	GRCh37 (hg19)		NC_000022.10	Chr22	46,501,286	46,501,286
essv16444913	Submitted genomic		NC_000022.10:g.465 01286_46501287ins?	GRCh37 (hg19)		NC_000022.10	Chr22	46,501,286	46,501,286
essv16444914	Submitted genomic		NC_000022.10:g.465 01286_46501287ins?	GRCh37 (hg19)		NC_000022.10	Chr22	46,501,286	46,501,286
essv16444915	Submitted genomic		NC_000022.10:g.465 01286_46501287ins?	GRCh37 (hg19)		NC_000022.10	Chr22	46,501,286	46,501,286
essv16444916	Submitted genomic		NC_000022.10:g.465 01286_46501287ins?	GRCh37 (hg19)		NC_000022.10	Chr22	46,501,286	46,501,286
essv16444917	Submitted genomic		NC_000022.10:g.465 01286_46501287ins?	GRCh37 (hg19)		NC_000022.10	Chr22	46,501,286	46,501,286
essv16444918	Submitted genomic		NC_000022.10:g.465 01286_46501287ins?	GRCh37 (hg19)		NC_000022.10	Chr22	46,501,286	46,501,286
essv16444919	Submitted genomic		NC_000022.10:g.465 01286_46501287ins?	GRCh37 (hg19)		NC_000022.10	Chr22	46,501,286	46,501,286
essv16444920	Submitted genomic		NC_000022.10:g.465 01286_46501287ins?	GRCh37 (hg19)		NC_000022.10	Chr22	46,501,286	46,501,286
essv16444921	Submitted genomic		NC_000022.10:g.465 01286_46501287ins?	GRCh37 (hg19)		NC_000022.10	Chr22	46,501,286	46,501,286
essv16444922	Submitted genomic		NC_000022.10:g.465 01286_46501287ins?	GRCh37 (hg19)		NC_000022.10	Chr22	46,501,286	46,501,286
essv16444923	Submitted genomic		NC_000022.10:g.465 01286_46501287ins?	GRCh37 (hg19)		NC_000022.10	Chr22	46,501,286	46,501,286
essv16444924	Submitted genomic		NC_000022.10:g.465 01286_46501287ins?	GRCh37 (hg19)		NC_000022.10	Chr22	46,501,286	46,501,286
essv16444925	Submitted genomic		NC_000022.10:g.465 01286_46501287ins?	GRCh37 (hg19)		NC_000022.10	Chr22	46,501,286	46,501,286
essv16444926	Submitted genomic		NC_000022.10:g.465 01286_46501287ins?	GRCh37 (hg19)		NC_000022.10	Chr22	46,501,286	46,501,286
essv16444927	Submitted genomic		NC_000022.10:g.465 01286_46501287ins?	GRCh37 (hg19)		NC_000022.10	Chr22	46,501,286	46,501,286
essv16444928	Submitted genomic		NC_000022.10:g.465 01286_46501287ins?	GRCh37 (hg19)		NC_000022.10	Chr22	46,501,286	46,501,286

Showing 100 of 102

dbVar

Database of genomic structural variation

esv3647941

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.