esv3647814

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: 123 SVs from 25 studies. See in: genome view

Remapped(Score: Perfect):42,237,099-42,237,099

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3647814	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
esv3647814	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000022.10	Chr22	42,633,105	42,633,105

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
essv16431111	alu insertion	SAMN00009254	Sequencing	Read depth and paired-end mapping	Heterozygous	2,508
essv16431112	alu insertion	SAMN00255125	Sequencing	Read depth and paired-end mapping	Heterozygous	3,547
essv16431113	alu insertion	SAMN00262992	Sequencing	Read depth and paired-end mapping	Heterozygous	3,290
essv16431114	alu insertion	SAMN00262980	Sequencing	Read depth and paired-end mapping	Heterozygous	2,988
essv16431115	alu insertion	SAMN00262983	Sequencing	Read depth and paired-end mapping	Heterozygous	3,036
essv16431116	alu insertion	SAMN00262984	Sequencing	Read depth and paired-end mapping	Heterozygous	3,090
essv16431117	alu insertion	SAMN00630223	Sequencing	Read depth and paired-end mapping	Heterozygous	3,177
essv16431118	alu insertion	SAMN00630235	Sequencing	Read depth and paired-end mapping	Heterozygous	3,253
essv16431119	alu insertion	SAMN00779937	Sequencing	Read depth and paired-end mapping	Heterozygous	3,210
essv16431120	alu insertion	SAMN01761208	Sequencing	Read depth and paired-end mapping	Heterozygous	3,316
essv16431121	alu insertion	SAMN01091059	Sequencing	Read depth and paired-end mapping	Heterozygous	2,925
essv16431122	alu insertion	SAMN00779949	Sequencing	Read depth and paired-end mapping	Heterozygous	3,105
essv16431123	alu insertion	SAMN00779952	Sequencing	Read depth and paired-end mapping	Heterozygous	3,140
essv16431124	alu insertion	SAMN01036703	Sequencing	Read depth and paired-end mapping	Heterozygous	3,162
essv16431125	alu insertion	SAMN01036707	Sequencing	Read depth and paired-end mapping	Heterozygous	3,285
essv16431126	alu insertion	SAMN00779979	Sequencing	Read depth and paired-end mapping	Heterozygous	3,212
essv16431127	alu insertion	SAMN01036734	Sequencing	Read depth and paired-end mapping	Heterozygous	2,930
essv16431128	alu insertion	SAMN01036737	Sequencing	Read depth and paired-end mapping	Heterozygous	2,966
essv16431129	alu insertion	SAMN01036769	Sequencing	Read depth and paired-end mapping	Heterozygous	2,858
essv16431130	alu insertion	SAMN01036775	Sequencing	Read depth and paired-end mapping	Heterozygous	3,028
essv16431131	alu insertion	SAMN01036797	Sequencing	Read depth and paired-end mapping	Heterozygous	3,180
essv16431132	alu insertion	SAMN01036800	Sequencing	Read depth and paired-end mapping	Heterozygous	3,246
essv16431133	alu insertion	SAMN01036748	Sequencing	Read depth and paired-end mapping	Heterozygous	3,191
essv16431134	alu insertion	SAMN01036754	Sequencing	Read depth and paired-end mapping	Heterozygous	3,219
essv16431135	alu insertion	SAMN01036779	Sequencing	Read depth and paired-end mapping	Heterozygous	3,152
essv16431136	alu insertion	SAMN01036780	Sequencing	Read depth and paired-end mapping	Heterozygous	3,149
essv16431137	alu insertion	SAMN01090874	Sequencing	Read depth and paired-end mapping	Heterozygous	3,163
essv16431138	alu insertion	SAMN01090774	Sequencing	Read depth and paired-end mapping	Heterozygous	3,029
essv16431139	alu insertion	SAMN01761323	Sequencing	Read depth and paired-end mapping	Heterozygous	3,121
essv16431140	alu insertion	SAMN01090780	Sequencing	Read depth and paired-end mapping	Heterozygous	3,063
essv16431141	alu insertion	SAMN01090781	Sequencing	Read depth and paired-end mapping	Heterozygous	3,088
essv16431142	alu insertion	SAMN01090783	Sequencing	Read depth and paired-end mapping	Heterozygous	2,989
essv16431143	alu insertion	SAMN01090786	Sequencing	Read depth and paired-end mapping	Heterozygous	3,121
essv16431144	alu insertion	SAMN01090788	Sequencing	Read depth and paired-end mapping	Heterozygous	3,127
essv16431145	alu insertion	SAMN01036789	Sequencing	Read depth and paired-end mapping	Heterozygous	3,228
essv16431146	alu insertion	SAMN00001577	Sequencing	Read depth and paired-end mapping	Heterozygous	3,105
essv16431147	alu insertion	SAMN00001585	Sequencing	Read depth and paired-end mapping	Heterozygous	3,075
essv16431148	alu insertion	SAMN00001589	Sequencing	Read depth and paired-end mapping	Heterozygous	3,170
essv16431149	alu insertion	SAMN00000475	Sequencing	Read depth and paired-end mapping	Heterozygous	3,336
essv16431150	alu insertion	SAMN00001631	Sequencing	Read depth and paired-end mapping	Heterozygous	3,116
essv16431151	alu insertion	SAMN00001040	Sequencing	Read depth and paired-end mapping	Heterozygous	3,220
essv16431152	alu insertion	SAMN00001046	Sequencing	Read depth and paired-end mapping	Heterozygous	3,260
essv16431153	alu insertion	SAMN00001048	Sequencing	Read depth and paired-end mapping	Heterozygous	3,061
essv16431154	alu insertion	SAMN00001054	Sequencing	Read depth and paired-end mapping	Heterozygous	3,219
essv16431155	alu insertion	SAMN00001057	Sequencing	Read depth and paired-end mapping	Heterozygous	3,084
essv16431156	alu insertion	SAMN00001059	Sequencing	Read depth and paired-end mapping	Heterozygous	3,175
essv16431157	alu insertion	SAMN00000547	Sequencing	Read depth and paired-end mapping	Heterozygous	3,222
essv16431158	alu insertion	SAMN00001672	Sequencing	Read depth and paired-end mapping	Heterozygous	2,981
essv16431159	alu insertion	SAMN00001678	Sequencing	Read depth and paired-end mapping	Heterozygous	3,261
essv16431160	alu insertion	SAMN00001679	Sequencing	Read depth and paired-end mapping	Heterozygous	2,977
essv16431161	alu insertion	SAMN00000573	Sequencing	Read depth and paired-end mapping	Heterozygous	3,050
essv16431162	alu insertion	SAMN00001102	Sequencing	Read depth and paired-end mapping	Heterozygous	2,846
essv16431163	alu insertion	SAMN00001111	Sequencing	Read depth and paired-end mapping	Heterozygous	2,426
essv16431164	alu insertion	SAMN00001121	Sequencing	Read depth and paired-end mapping	Heterozygous	3,030
essv16431165	alu insertion	SAMN00001123	Sequencing	Read depth and paired-end mapping	Homozygous	3,160
essv16431166	alu insertion	SAMN00001132	Sequencing	Read depth and paired-end mapping	Heterozygous	2,992
essv16431167	alu insertion	SAMN00001134	Sequencing	Read depth and paired-end mapping	Homozygous	2,950
essv16431168	alu insertion	SAMN00001135	Sequencing	Read depth and paired-end mapping	Heterozygous	3,038
essv16431169	alu insertion	SAMN00001137	Sequencing	Read depth and paired-end mapping	Heterozygous	3,195
essv16431170	alu insertion	SAMN00001146	Sequencing	Read depth and paired-end mapping	Heterozygous	3,120
essv16431171	alu insertion	SAMN00001147	Sequencing	Read depth and paired-end mapping	Heterozygous	3,043
essv16431172	alu insertion	SAMN00001148	Sequencing	Read depth and paired-end mapping	Heterozygous	2,889
essv16431173	alu insertion	SAMN00001162	Sequencing	Read depth and paired-end mapping	Heterozygous	2,775
essv16431174	alu insertion	SAMN00001175	Sequencing	Read depth and paired-end mapping	Heterozygous	2,829
essv16431175	alu insertion	SAMN00001183	Sequencing	Read depth and paired-end mapping	Heterozygous	2,986
essv16431176	alu insertion	SAMN00007700	Sequencing	Read depth and paired-end mapping	Heterozygous	3,096
essv16431177	alu insertion	SAMN00007738	Sequencing	Read depth and paired-end mapping	Heterozygous	3,051

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv16431111	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431112	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431113	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431114	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431115	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431116	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431117	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431118	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431119	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431120	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431121	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431122	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431123	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431124	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431125	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431126	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431127	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431128	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431129	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431130	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431131	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431132	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431133	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431134	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431135	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431136	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431137	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431138	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431139	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431140	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431141	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431142	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431143	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431144	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431145	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431146	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431147	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431148	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431149	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431150	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431151	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431152	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431153	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431154	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431155	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431156	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431157	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431158	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431159	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431160	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431161	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431162	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431163	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431164	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431165	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431166	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431167	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431168	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431169	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431170	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431171	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431172	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431173	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431174	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431175	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431176	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431177	Remapped	Perfect	NC_000022.11:g.422 37099_42237100ins?	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,237,099	42,237,099
essv16431111	Submitted genomic		NC_000022.10:g.426 33105_42633106ins?	GRCh37 (hg19)		NC_000022.10	Chr22	42,633,105	42,633,105
essv16431112	Submitted genomic		NC_000022.10:g.426 33105_42633106ins?	GRCh37 (hg19)		NC_000022.10	Chr22	42,633,105	42,633,105
essv16431113	Submitted genomic		NC_000022.10:g.426 33105_42633106ins?	GRCh37 (hg19)		NC_000022.10	Chr22	42,633,105	42,633,105
essv16431114	Submitted genomic		NC_000022.10:g.426 33105_42633106ins?	GRCh37 (hg19)		NC_000022.10	Chr22	42,633,105	42,633,105
essv16431115	Submitted genomic		NC_000022.10:g.426 33105_42633106ins?	GRCh37 (hg19)		NC_000022.10	Chr22	42,633,105	42,633,105
essv16431116	Submitted genomic		NC_000022.10:g.426 33105_42633106ins?	GRCh37 (hg19)		NC_000022.10	Chr22	42,633,105	42,633,105
essv16431117	Submitted genomic		NC_000022.10:g.426 33105_42633106ins?	GRCh37 (hg19)		NC_000022.10	Chr22	42,633,105	42,633,105
essv16431118	Submitted genomic		NC_000022.10:g.426 33105_42633106ins?	GRCh37 (hg19)		NC_000022.10	Chr22	42,633,105	42,633,105
essv16431119	Submitted genomic		NC_000022.10:g.426 33105_42633106ins?	GRCh37 (hg19)		NC_000022.10	Chr22	42,633,105	42,633,105
essv16431120	Submitted genomic		NC_000022.10:g.426 33105_42633106ins?	GRCh37 (hg19)		NC_000022.10	Chr22	42,633,105	42,633,105
essv16431121	Submitted genomic		NC_000022.10:g.426 33105_42633106ins?	GRCh37 (hg19)		NC_000022.10	Chr22	42,633,105	42,633,105
essv16431122	Submitted genomic		NC_000022.10:g.426 33105_42633106ins?	GRCh37 (hg19)		NC_000022.10	Chr22	42,633,105	42,633,105
essv16431123	Submitted genomic		NC_000022.10:g.426 33105_42633106ins?	GRCh37 (hg19)		NC_000022.10	Chr22	42,633,105	42,633,105
essv16431124	Submitted genomic		NC_000022.10:g.426 33105_42633106ins?	GRCh37 (hg19)		NC_000022.10	Chr22	42,633,105	42,633,105
essv16431125	Submitted genomic		NC_000022.10:g.426 33105_42633106ins?	GRCh37 (hg19)		NC_000022.10	Chr22	42,633,105	42,633,105
essv16431126	Submitted genomic		NC_000022.10:g.426 33105_42633106ins?	GRCh37 (hg19)		NC_000022.10	Chr22	42,633,105	42,633,105
essv16431127	Submitted genomic		NC_000022.10:g.426 33105_42633106ins?	GRCh37 (hg19)		NC_000022.10	Chr22	42,633,105	42,633,105
essv16431128	Submitted genomic		NC_000022.10:g.426 33105_42633106ins?	GRCh37 (hg19)		NC_000022.10	Chr22	42,633,105	42,633,105
essv16431129	Submitted genomic		NC_000022.10:g.426 33105_42633106ins?	GRCh37 (hg19)		NC_000022.10	Chr22	42,633,105	42,633,105
essv16431130	Submitted genomic		NC_000022.10:g.426 33105_42633106ins?	GRCh37 (hg19)		NC_000022.10	Chr22	42,633,105	42,633,105
essv16431131	Submitted genomic		NC_000022.10:g.426 33105_42633106ins?	GRCh37 (hg19)		NC_000022.10	Chr22	42,633,105	42,633,105
essv16431132	Submitted genomic		NC_000022.10:g.426 33105_42633106ins?	GRCh37 (hg19)		NC_000022.10	Chr22	42,633,105	42,633,105
essv16431133	Submitted genomic		NC_000022.10:g.426 33105_42633106ins?	GRCh37 (hg19)		NC_000022.10	Chr22	42,633,105	42,633,105
essv16431134	Submitted genomic		NC_000022.10:g.426 33105_42633106ins?	GRCh37 (hg19)		NC_000022.10	Chr22	42,633,105	42,633,105
essv16431135	Submitted genomic		NC_000022.10:g.426 33105_42633106ins?	GRCh37 (hg19)		NC_000022.10	Chr22	42,633,105	42,633,105
essv16431136	Submitted genomic		NC_000022.10:g.426 33105_42633106ins?	GRCh37 (hg19)		NC_000022.10	Chr22	42,633,105	42,633,105
essv16431137	Submitted genomic		NC_000022.10:g.426 33105_42633106ins?	GRCh37 (hg19)		NC_000022.10	Chr22	42,633,105	42,633,105
essv16431138	Submitted genomic		NC_000022.10:g.426 33105_42633106ins?	GRCh37 (hg19)		NC_000022.10	Chr22	42,633,105	42,633,105
essv16431139	Submitted genomic		NC_000022.10:g.426 33105_42633106ins?	GRCh37 (hg19)		NC_000022.10	Chr22	42,633,105	42,633,105
essv16431140	Submitted genomic		NC_000022.10:g.426 33105_42633106ins?	GRCh37 (hg19)		NC_000022.10	Chr22	42,633,105	42,633,105
essv16431141	Submitted genomic		NC_000022.10:g.426 33105_42633106ins?	GRCh37 (hg19)		NC_000022.10	Chr22	42,633,105	42,633,105
essv16431142	Submitted genomic		NC_000022.10:g.426 33105_42633106ins?	GRCh37 (hg19)		NC_000022.10	Chr22	42,633,105	42,633,105
essv16431143	Submitted genomic		NC_000022.10:g.426 33105_42633106ins?	GRCh37 (hg19)		NC_000022.10	Chr22	42,633,105	42,633,105

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dbVar

Database of genomic structural variation

esv3647814

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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.