esv3647869

Organism: Homo sapiens

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

Variant Calls:58
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: 176 SVs from 31 studies. See in: genome view

Remapped(Score: Perfect):43,497,770-43,497,770

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3647869	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
esv3647869	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000022.10	Chr22	43,893,650	43,893,650

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
essv16435723	alu insertion	SAMN01091079	Sequencing	Read depth and paired-end mapping	Heterozygous	2,318
essv16435724	alu insertion	SAMN00009117	Sequencing	Read depth and paired-end mapping	Heterozygous	2,753
essv16435725	alu insertion	SAMN00009199	Sequencing	Read depth and paired-end mapping	Heterozygous	2,710
essv16435726	alu insertion	SAMN01091063	Sequencing	Read depth and paired-end mapping	Heterozygous	2,691
essv16435727	alu insertion	SAMN00255125	Sequencing	Read depth and paired-end mapping	Heterozygous	3,547
essv16435728	alu insertion	SAMN00262993	Sequencing	Read depth and paired-end mapping	Heterozygous	3,311
essv16435729	alu insertion	SAMN00630209	Sequencing	Read depth and paired-end mapping	Heterozygous	3,050
essv16435730	alu insertion	SAMN00630222	Sequencing	Read depth and paired-end mapping	Heterozygous	3,114
essv16435731	alu insertion	SAMN00630224	Sequencing	Read depth and paired-end mapping	Heterozygous	3,117
essv16435732	alu insertion	SAMN00630236	Sequencing	Read depth and paired-end mapping	Heterozygous	3,237
essv16435733	alu insertion	SAMN01091045	Sequencing	Read depth and paired-end mapping	Heterozygous	3,089
essv16435734	alu insertion	SAMN00630249	Sequencing	Read depth and paired-end mapping	Heterozygous	2,770
essv16435735	alu insertion	SAMN01091054	Sequencing	Read depth and paired-end mapping	Heterozygous	3,333
essv16435736	alu insertion	SAMN00779937	Sequencing	Read depth and paired-end mapping	Heterozygous	3,210
essv16435737	alu insertion	SAMN00779939	Sequencing	Read depth and paired-end mapping	Heterozygous	3,238
essv16435738	alu insertion	SAMN00779949	Sequencing	Read depth and paired-end mapping	Heterozygous	3,105
essv16435739	alu insertion	SAMN00779964	Sequencing	Read depth and paired-end mapping	Heterozygous	3,151
essv16435740	alu insertion	SAMN01036706	Sequencing	Read depth and paired-end mapping	Heterozygous	3,223
essv16435741	alu insertion	SAMN01036718	Sequencing	Read depth and paired-end mapping	Heterozygous	3,203
essv16435742	alu insertion	SAMN01036721	Sequencing	Read depth and paired-end mapping	Heterozygous	3,162
essv16435743	alu insertion	SAMN01761272	Sequencing	Read depth and paired-end mapping	Heterozygous	3,508
essv16435744	alu insertion	SAMN01090864	Sequencing	Read depth and paired-end mapping	Heterozygous	2,852
essv16435745	alu insertion	SAMN01090798	Sequencing	Read depth and paired-end mapping	Heterozygous	3,064
essv16435746	alu insertion	SAMN01036810	Sequencing	Read depth and paired-end mapping	Heterozygous	3,221
essv16435747	alu insertion	SAMN01761293	Sequencing	Read depth and paired-end mapping	Heterozygous	3,440
essv16435748	alu insertion	SAMN01036819	Sequencing	Read depth and paired-end mapping	Heterozygous	3,300
essv16435749	alu insertion	SAMN01036822	Sequencing	Read depth and paired-end mapping	Heterozygous	3,231
essv16435750	alu insertion	SAMN01761302	Sequencing	Read depth and paired-end mapping	Heterozygous	3,284
essv16435751	alu insertion	SAMN01090774	Sequencing	Read depth and paired-end mapping	Heterozygous	3,029
essv16435752	alu insertion	SAMN01090818	Sequencing	Read depth and paired-end mapping	Heterozygous	3,288
essv16435753	alu insertion	SAMN01090781	Sequencing	Read depth and paired-end mapping	Heterozygous	3,088
essv16435754	alu insertion	SAMN01036788	Sequencing	Read depth and paired-end mapping	Heterozygous	3,166
essv16435755	alu insertion	SAMN01036791	Sequencing	Read depth and paired-end mapping	Heterozygous	3,202
essv16435756	alu insertion	SAMN01090809	Sequencing	Read depth and paired-end mapping	Heterozygous	3,083
essv16435757	alu insertion	SAMN01761353	Sequencing	Read depth and paired-end mapping	Heterozygous	3,438
essv16435758	alu insertion	SAMN01090823	Sequencing	Read depth and paired-end mapping	Heterozygous	3,198
essv16435759	alu insertion	SAMN00001585	Sequencing	Read depth and paired-end mapping	Heterozygous	3,075
essv16435760	alu insertion	SAMN00001625	Sequencing	Read depth and paired-end mapping	Heterozygous	3,281
essv16435761	alu insertion	SAMN00001626	Sequencing	Read depth and paired-end mapping	Heterozygous	3,243
essv16435762	alu insertion	SAMN00001627	Sequencing	Read depth and paired-end mapping	Heterozygous	3,105
essv16435763	alu insertion	SAMN00000477	Sequencing	Read depth and paired-end mapping	Heterozygous	3,404
essv16435764	alu insertion	SAMN00001021	Sequencing	Read depth and paired-end mapping	Heterozygous	3,301
essv16435765	alu insertion	SAMN00000478	Sequencing	Read depth and paired-end mapping	Heterozygous	3,327
essv16435766	alu insertion	SAMN00001059	Sequencing	Read depth and paired-end mapping	Heterozygous	3,175
essv16435767	alu insertion	SAMN00001667	Sequencing	Read depth and paired-end mapping	Heterozygous	3,266
essv16435768	alu insertion	SAMN00000550	Sequencing	Read depth and paired-end mapping	Heterozygous	3,070
essv16435769	alu insertion	SAMN00001683	Sequencing	Read depth and paired-end mapping	Heterozygous	2,908
essv16435770	alu insertion	SAMN00000563	Sequencing	Read depth and paired-end mapping	Heterozygous	3,273
essv16435771	alu insertion	SAMN00000569	Sequencing	Read depth and paired-end mapping	Heterozygous	2,809
essv16435772	alu insertion	SAMN00001119	Sequencing	Read depth and paired-end mapping	Heterozygous	3,113
essv16435773	alu insertion	SAMN00001122	Sequencing	Read depth and paired-end mapping	Heterozygous	3,250
essv16435774	alu insertion	SAMN00007737	Sequencing	Read depth and paired-end mapping	Heterozygous	3,041
essv16435775	alu insertion	SAMN00007806	Sequencing	Read depth and paired-end mapping	Heterozygous	3,302
essv16435776	alu insertion	SAMN00007807	Sequencing	Read depth and paired-end mapping	Heterozygous	3,277
essv16435777	alu insertion	SAMN00007810	Sequencing	Read depth and paired-end mapping	Heterozygous	3,058
essv16435778	alu insertion	SAMN00007812	Sequencing	Read depth and paired-end mapping	Heterozygous	3,129
essv16435779	alu insertion	SAMN00007870	Sequencing	Read depth and paired-end mapping	Heterozygous	2,441
essv16435780	alu insertion	SAMN00007873	Sequencing	Read depth and paired-end mapping	Heterozygous	2,690

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv16435723	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435724	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435725	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435726	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435727	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435728	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435729	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435730	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435731	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435732	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435733	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435734	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435735	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435736	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435737	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435738	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435739	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435740	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435741	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435742	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435743	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435744	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435745	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435746	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435747	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435748	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435749	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435750	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435751	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435752	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435753	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435754	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435755	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435756	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435757	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435758	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435759	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435760	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435761	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435762	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435763	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435764	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435765	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435766	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435767	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435768	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435769	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435770	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435771	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435772	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435773	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435774	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435775	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435776	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435777	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435778	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435779	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435780	Remapped	Perfect	NC_000022.11:g.434 97770_43497771ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	43,497,770	43,497,770
essv16435723	Submitted genomic		NC_000022.10:g.438 93650_43893651ins?	GRCh37 (hg19)		NC_000022.10	Chr22	43,893,650	43,893,650
essv16435724	Submitted genomic		NC_000022.10:g.438 93650_43893651ins?	GRCh37 (hg19)		NC_000022.10	Chr22	43,893,650	43,893,650
essv16435725	Submitted genomic		NC_000022.10:g.438 93650_43893651ins?	GRCh37 (hg19)		NC_000022.10	Chr22	43,893,650	43,893,650
essv16435726	Submitted genomic		NC_000022.10:g.438 93650_43893651ins?	GRCh37 (hg19)		NC_000022.10	Chr22	43,893,650	43,893,650
essv16435727	Submitted genomic		NC_000022.10:g.438 93650_43893651ins?	GRCh37 (hg19)		NC_000022.10	Chr22	43,893,650	43,893,650
essv16435728	Submitted genomic		NC_000022.10:g.438 93650_43893651ins?	GRCh37 (hg19)		NC_000022.10	Chr22	43,893,650	43,893,650
essv16435729	Submitted genomic		NC_000022.10:g.438 93650_43893651ins?	GRCh37 (hg19)		NC_000022.10	Chr22	43,893,650	43,893,650
essv16435730	Submitted genomic		NC_000022.10:g.438 93650_43893651ins?	GRCh37 (hg19)		NC_000022.10	Chr22	43,893,650	43,893,650
essv16435731	Submitted genomic		NC_000022.10:g.438 93650_43893651ins?	GRCh37 (hg19)		NC_000022.10	Chr22	43,893,650	43,893,650
essv16435732	Submitted genomic		NC_000022.10:g.438 93650_43893651ins?	GRCh37 (hg19)		NC_000022.10	Chr22	43,893,650	43,893,650
essv16435733	Submitted genomic		NC_000022.10:g.438 93650_43893651ins?	GRCh37 (hg19)		NC_000022.10	Chr22	43,893,650	43,893,650
essv16435734	Submitted genomic		NC_000022.10:g.438 93650_43893651ins?	GRCh37 (hg19)		NC_000022.10	Chr22	43,893,650	43,893,650
essv16435735	Submitted genomic		NC_000022.10:g.438 93650_43893651ins?	GRCh37 (hg19)		NC_000022.10	Chr22	43,893,650	43,893,650
essv16435736	Submitted genomic		NC_000022.10:g.438 93650_43893651ins?	GRCh37 (hg19)		NC_000022.10	Chr22	43,893,650	43,893,650
essv16435737	Submitted genomic		NC_000022.10:g.438 93650_43893651ins?	GRCh37 (hg19)		NC_000022.10	Chr22	43,893,650	43,893,650
essv16435738	Submitted genomic		NC_000022.10:g.438 93650_43893651ins?	GRCh37 (hg19)		NC_000022.10	Chr22	43,893,650	43,893,650
essv16435739	Submitted genomic		NC_000022.10:g.438 93650_43893651ins?	GRCh37 (hg19)		NC_000022.10	Chr22	43,893,650	43,893,650
essv16435740	Submitted genomic		NC_000022.10:g.438 93650_43893651ins?	GRCh37 (hg19)		NC_000022.10	Chr22	43,893,650	43,893,650
essv16435741	Submitted genomic		NC_000022.10:g.438 93650_43893651ins?	GRCh37 (hg19)		NC_000022.10	Chr22	43,893,650	43,893,650
essv16435742	Submitted genomic		NC_000022.10:g.438 93650_43893651ins?	GRCh37 (hg19)		NC_000022.10	Chr22	43,893,650	43,893,650
essv16435743	Submitted genomic		NC_000022.10:g.438 93650_43893651ins?	GRCh37 (hg19)		NC_000022.10	Chr22	43,893,650	43,893,650
essv16435744	Submitted genomic		NC_000022.10:g.438 93650_43893651ins?	GRCh37 (hg19)		NC_000022.10	Chr22	43,893,650	43,893,650
essv16435745	Submitted genomic		NC_000022.10:g.438 93650_43893651ins?	GRCh37 (hg19)		NC_000022.10	Chr22	43,893,650	43,893,650
essv16435746	Submitted genomic		NC_000022.10:g.438 93650_43893651ins?	GRCh37 (hg19)		NC_000022.10	Chr22	43,893,650	43,893,650
essv16435747	Submitted genomic		NC_000022.10:g.438 93650_43893651ins?	GRCh37 (hg19)		NC_000022.10	Chr22	43,893,650	43,893,650
essv16435748	Submitted genomic		NC_000022.10:g.438 93650_43893651ins?	GRCh37 (hg19)		NC_000022.10	Chr22	43,893,650	43,893,650
essv16435749	Submitted genomic		NC_000022.10:g.438 93650_43893651ins?	GRCh37 (hg19)		NC_000022.10	Chr22	43,893,650	43,893,650
essv16435750	Submitted genomic		NC_000022.10:g.438 93650_43893651ins?	GRCh37 (hg19)		NC_000022.10	Chr22	43,893,650	43,893,650
essv16435751	Submitted genomic		NC_000022.10:g.438 93650_43893651ins?	GRCh37 (hg19)		NC_000022.10	Chr22	43,893,650	43,893,650
essv16435752	Submitted genomic		NC_000022.10:g.438 93650_43893651ins?	GRCh37 (hg19)		NC_000022.10	Chr22	43,893,650	43,893,650
essv16435753	Submitted genomic		NC_000022.10:g.438 93650_43893651ins?	GRCh37 (hg19)		NC_000022.10	Chr22	43,893,650	43,893,650
essv16435754	Submitted genomic		NC_000022.10:g.438 93650_43893651ins?	GRCh37 (hg19)		NC_000022.10	Chr22	43,893,650	43,893,650
essv16435755	Submitted genomic		NC_000022.10:g.438 93650_43893651ins?	GRCh37 (hg19)		NC_000022.10	Chr22	43,893,650	43,893,650
essv16435756	Submitted genomic		NC_000022.10:g.438 93650_43893651ins?	GRCh37 (hg19)		NC_000022.10	Chr22	43,893,650	43,893,650
essv16435757	Submitted genomic		NC_000022.10:g.438 93650_43893651ins?	GRCh37 (hg19)		NC_000022.10	Chr22	43,893,650	43,893,650
essv16435758	Submitted genomic		NC_000022.10:g.438 93650_43893651ins?	GRCh37 (hg19)		NC_000022.10	Chr22	43,893,650	43,893,650
essv16435759	Submitted genomic		NC_000022.10:g.438 93650_43893651ins?	GRCh37 (hg19)		NC_000022.10	Chr22	43,893,650	43,893,650
essv16435760	Submitted genomic		NC_000022.10:g.438 93650_43893651ins?	GRCh37 (hg19)		NC_000022.10	Chr22	43,893,650	43,893,650
essv16435761	Submitted genomic		NC_000022.10:g.438 93650_43893651ins?	GRCh37 (hg19)		NC_000022.10	Chr22	43,893,650	43,893,650
essv16435762	Submitted genomic		NC_000022.10:g.438 93650_43893651ins?	GRCh37 (hg19)		NC_000022.10	Chr22	43,893,650	43,893,650
essv16435763	Submitted genomic		NC_000022.10:g.438 93650_43893651ins?	GRCh37 (hg19)		NC_000022.10	Chr22	43,893,650	43,893,650
essv16435764	Submitted genomic		NC_000022.10:g.438 93650_43893651ins?	GRCh37 (hg19)		NC_000022.10	Chr22	43,893,650	43,893,650

Showing 100 of 116

dbVar

Database of genomic structural variation

esv3647869

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.