esv3624746

Organism: Homo sapiens

Study:estd214 (1000 Genomes Consortium Phase 3)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh37

Variant Calls:147
Validation:Not tested
Clinical Assertions: No
Region Size:17,801

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: 268 SVs from 55 studies. See in: genome view

Remapped(Score: Perfect):121,010,189-121,027,991

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3624746	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
esv3624746	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000010.10	Chr10	122,769,703 (-1, +1)	122,787,503 (-1, +1)

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
essv13952694	deletion	SAMN00009114	Sequencing	Read depth and paired-end mapping	Heterozygous	2,651
essv13952695	deletion	SAMN00006535	Sequencing	Read depth and paired-end mapping	Heterozygous	2,682
essv13952696	deletion	SAMN01091061	Sequencing	Read depth and paired-end mapping	Heterozygous	2,698
essv13952697	deletion	SAMN01091085	Sequencing	Read depth and paired-end mapping	Heterozygous	2,184
essv13952698	deletion	SAMN00009139	Sequencing	Read depth and paired-end mapping	Heterozygous	2,788
essv13952699	deletion	SAMN01091086	Sequencing	Read depth and paired-end mapping	Heterozygous	2,326
essv13952700	deletion	SAMN00009199	Sequencing	Read depth and paired-end mapping	Heterozygous	2,710
essv13952701	deletion	SAMN01091110	Sequencing	Read depth and paired-end mapping	Heterozygous	2,641
essv13952702	deletion	SAMN00014396	Sequencing	Read depth and paired-end mapping	Heterozygous	2,329
essv13952703	deletion	SAMN00249685	Sequencing	Read depth and paired-end mapping	Heterozygous	2,730
essv13952704	deletion	SAMN00630202	Sequencing	Read depth and paired-end mapping	Heterozygous	3,111
essv13952705	deletion	SAMN00630209	Sequencing	Read depth and paired-end mapping	Homozygous	3,050
essv13952706	deletion	SAMN00262986	Sequencing	Read depth and paired-end mapping	Heterozygous	3,389
essv13952707	deletion	SAMN00630215	Sequencing	Read depth and paired-end mapping	Heterozygous	3,137
essv13952708	deletion	SAMN00630224	Sequencing	Read depth and paired-end mapping	Heterozygous	3,117
essv13952709	deletion	SAMN00630226	Sequencing	Read depth and paired-end mapping	Heterozygous	3,053
essv13952710	deletion	SAMN00630234	Sequencing	Read depth and paired-end mapping	Heterozygous	3,182
essv13952711	deletion	SAMN00630236	Sequencing	Read depth and paired-end mapping	Heterozygous	3,237
essv13952712	deletion	SAMN00779930	Sequencing	Read depth and paired-end mapping	Heterozygous	3,244
essv13952713	deletion	SAMN01091044	Sequencing	Read depth and paired-end mapping	Heterozygous	2,852
essv13952714	deletion	SAMN00630250	Sequencing	Read depth and paired-end mapping	Heterozygous	2,763
essv13952715	deletion	SAMN01091049	Sequencing	Read depth and paired-end mapping	Heterozygous	2,372
essv13952716	deletion	SAMN00630253	Sequencing	Read depth and paired-end mapping	Heterozygous	3,391
essv13952717	deletion	SAMN01091051	Sequencing	Read depth and paired-end mapping	Heterozygous	3,290
essv13952718	deletion	SAMN00779936	Sequencing	Read depth and paired-end mapping	Heterozygous	3,103
essv13952719	deletion	SAMN00779937	Sequencing	Read depth and paired-end mapping	Heterozygous	3,210
essv13952720	deletion	SAMN00779939	Sequencing	Read depth and paired-end mapping	Heterozygous	3,238
essv13952721	deletion	SAMN00779942	Sequencing	Read depth and paired-end mapping	Heterozygous	3,199
essv13952722	deletion	SAMN00779948	Sequencing	Read depth and paired-end mapping	Heterozygous	3,126
essv13952723	deletion	SAMN01036704	Sequencing	Read depth and paired-end mapping	Heterozygous	3,279
essv13952724	deletion	SAMN00779960	Sequencing	Read depth and paired-end mapping	Heterozygous	3,258
essv13952725	deletion	SAMN00779972	Sequencing	Read depth and paired-end mapping	Heterozygous	3,233
essv13952726	deletion	SAMN00779975	Sequencing	Read depth and paired-end mapping	Homozygous	3,186
essv13952727	deletion	SAMN00779981	Sequencing	Read depth and paired-end mapping	Homozygous	3,163
essv13952728	deletion	SAMN01036710	Sequencing	Read depth and paired-end mapping	Heterozygous	3,268
essv13952729	deletion	SAMN00779988	Sequencing	Read depth and paired-end mapping	Heterozygous	3,242
essv13952730	deletion	SAMN01761210	Sequencing	Read depth and paired-end mapping	Heterozygous	3,236
essv13952731	deletion	SAMN01036718	Sequencing	Read depth and paired-end mapping	Heterozygous	3,203
essv13952732	deletion	SAMN01036719	Sequencing	Read depth and paired-end mapping	Heterozygous	3,186
essv13952733	deletion	SAMN01036767	Sequencing	Read depth and paired-end mapping	Heterozygous	3,001
essv13952734	deletion	SAMN01036733	Sequencing	Read depth and paired-end mapping	Heterozygous	3,100
essv13952735	deletion	SAMN01036769	Sequencing	Read depth and paired-end mapping	Heterozygous	2,858
essv13952736	deletion	SAMN01761217	Sequencing	Read depth and paired-end mapping	Heterozygous	2,482
essv13952737	deletion	SAMN01036772	Sequencing	Read depth and paired-end mapping	Heterozygous	2,974
essv13952738	deletion	SAMN01036739	Sequencing	Read depth and paired-end mapping	Heterozygous	2,952
essv13952739	deletion	SAMN01036742	Sequencing	Read depth and paired-end mapping	Heterozygous	2,959
essv13952740	deletion	SAMN01090865	Sequencing	Read depth and paired-end mapping	Heterozygous	2,879
essv13952741	deletion	SAMN01761226	Sequencing	Read depth and paired-end mapping	Heterozygous	3,196
essv13952742	deletion	SAMN01090748	Sequencing	Read depth and paired-end mapping	Heterozygous	2,921
essv13952743	deletion	SAMN01036748	Sequencing	Read depth and paired-end mapping	Heterozygous	3,191
essv13952744	deletion	SAMN01036755	Sequencing	Read depth and paired-end mapping	Heterozygous	3,248
essv13952745	deletion	SAMN01036778	Sequencing	Read depth and paired-end mapping	Heterozygous	3,213
essv13952746	deletion	SAMN01036779	Sequencing	Read depth and paired-end mapping	Heterozygous	3,152
essv13952747	deletion	SAMN01090784	Sequencing	Read depth and paired-end mapping	Heterozygous	2,819
essv13952748	deletion	SAMN01761234	Sequencing	Read depth and paired-end mapping	Heterozygous	3,228
essv13952749	deletion	SAMN01761240	Sequencing	Read depth and paired-end mapping	Heterozygous	3,309
essv13952750	deletion	SAMN01036782	Sequencing	Read depth and paired-end mapping	Heterozygous	3,182
essv13952751	deletion	SAMN01036785	Sequencing	Read depth and paired-end mapping	Heterozygous	3,177
essv13952752	deletion	SAMN01761293	Sequencing	Read depth and paired-end mapping	Heterozygous	3,440
essv13952753	deletion	SAMN01036818	Sequencing	Read depth and paired-end mapping	Heterozygous	3,167
essv13952754	deletion	SAMN01761302	Sequencing	Read depth and paired-end mapping	Heterozygous	3,284
essv13952755	deletion	SAMN01761304	Sequencing	Read depth and paired-end mapping	Heterozygous	3,309
essv13952756	deletion	SAMN01090892	Sequencing	Read depth and paired-end mapping	Heterozygous	2,959
essv13952757	deletion	SAMN01090891	Sequencing	Read depth and paired-end mapping	Heterozygous	3,001
essv13952758	deletion	SAMN01761247	Sequencing	Read depth and paired-end mapping	Heterozygous	3,183
essv13952759	deletion	SAMN01090754	Sequencing	Read depth and paired-end mapping	Heterozygous	2,921
essv13952760	deletion	SAMN01761316	Sequencing	Read depth and paired-end mapping	Heterozygous	3,322
essv13952761	deletion	SAMN01090853	Sequencing	Read depth and paired-end mapping	Heterozygous	2,890
essv13952762	deletion	SAMN01761323	Sequencing	Read depth and paired-end mapping	Heterozygous	3,121
essv13952763	deletion	SAMN01761329	Sequencing	Read depth and paired-end mapping	Heterozygous	2,537
essv13952764	deletion	SAMN01090859	Sequencing	Read depth and paired-end mapping	Heterozygous	2,807
essv13952765	deletion	SAMN01090901	Sequencing	Read depth and paired-end mapping	Heterozygous	3,003
essv13952766	deletion	SAMN01761248	Sequencing	Read depth and paired-end mapping	Heterozygous	3,116
essv13952767	deletion	SAMN01761259	Sequencing	Read depth and paired-end mapping	Heterozygous	2,594
essv13952768	deletion	SAMN01090802	Sequencing	Read depth and paired-end mapping	Heterozygous	2,849
essv13952769	deletion	SAMN01090787	Sequencing	Read depth and paired-end mapping	Heterozygous	3,193
essv13952770	deletion	SAMN01090789	Sequencing	Read depth and paired-end mapping	Heterozygous	3,152
essv13952771	deletion	SAMN01036789	Sequencing	Read depth and paired-end mapping	Heterozygous	3,228
essv13952772	deletion	SAMN01090820	Sequencing	Read depth and paired-end mapping	Heterozygous	3,024
essv13952773	deletion	SAMN01036792	Sequencing	Read depth and paired-end mapping	Heterozygous	2,941
essv13952774	deletion	SAMN01090768	Sequencing	Read depth and paired-end mapping	Heterozygous	3,030
essv13952775	deletion	SAMN01090793	Sequencing	Read depth and paired-end mapping	Heterozygous	2,951
essv13952776	deletion	SAMN01761348	Sequencing	Read depth and paired-end mapping	Homozygous	3,263
essv13952777	deletion	SAMN01761353	Sequencing	Read depth and paired-end mapping	Heterozygous	3,438
essv13952778	deletion	SAMN01090822	Sequencing	Read depth and paired-end mapping	Heterozygous	3,090
essv13952779	deletion	SAMN00001586	Sequencing	Read depth and paired-end mapping	Heterozygous	3,256
essv13952780	deletion	SAMN00001587	Sequencing	Read depth and paired-end mapping	Heterozygous	2,644
essv13952781	deletion	SAMN00001623	Sequencing	Read depth and paired-end mapping	Heterozygous	3,153
essv13952782	deletion	SAMN00000474	Sequencing	Read depth and paired-end mapping	Heterozygous	3,015
essv13952783	deletion	SAMN00001627	Sequencing	Read depth and paired-end mapping	Heterozygous	3,105
essv13952784	deletion	SAMN00000477	Sequencing	Read depth and paired-end mapping	Heterozygous	3,404
essv13952785	deletion	SAMN00001022	Sequencing	Read depth and paired-end mapping	Heterozygous	3,306
essv13952786	deletion	SAMN00001630	Sequencing	Read depth and paired-end mapping	Heterozygous	3,334
essv13952787	deletion	SAMN00001632	Sequencing	Read depth and paired-end mapping	Heterozygous	3,256
essv13952788	deletion	SAMN00000482	Sequencing	Read depth and paired-end mapping	Heterozygous	2,317
essv13952789	deletion	SAMN00000483	Sequencing	Read depth and paired-end mapping	Heterozygous	2,460
essv13952790	deletion	SAMN00001044	Sequencing	Read depth and paired-end mapping	Homozygous	3,190
essv13952791	deletion	SAMN00001051	Sequencing	Read depth and paired-end mapping	Heterozygous	2,862
essv13952792	deletion	SAMN00001052	Sequencing	Read depth and paired-end mapping	Heterozygous	3,055
essv13952793	deletion	SAMN00000547	Sequencing	Read depth and paired-end mapping	Heterozygous	3,222

Showing 100 of 147

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv13952694	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952695	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952696	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952697	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952698	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952699	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952700	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952701	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952702	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952703	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952704	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952705	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952706	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952707	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952708	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952709	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952710	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952711	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952712	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952713	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952714	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952715	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952716	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952717	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952718	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952719	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952720	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952721	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952722	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952723	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952724	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952725	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952726	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952727	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952728	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952729	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952730	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952731	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952732	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952733	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952734	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952735	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952736	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952737	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952738	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952739	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952740	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952741	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952742	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952743	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952744	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952745	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952746	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952747	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952748	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952749	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952750	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952751	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952752	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952753	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952754	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952755	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952756	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952757	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952758	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952759	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952760	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952761	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952762	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952763	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952764	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952765	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952766	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952767	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952768	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952769	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952770	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952771	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952772	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952773	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952774	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952775	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952776	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952777	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952778	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952779	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952780	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952781	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952782	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952783	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952784	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952785	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952786	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952787	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952788	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952789	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952790	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952791	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952792	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)
essv13952793	Remapped	Perfect	NC_000010.11:g.(12 1010189_121010191) _(121027989_121027 991)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	121,010,190 (-1, +1)	121,027,990 (-1, +1)

Showing 100 of 294

dbVar

Database of genomic structural variation

esv3624746

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.