esv3821564

Organism: Homo sapiens

Study:estd219 (1000 Genomes Consortium Phase 3 Integrated SV)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh37

Variant Calls:50
Validation:Not tested
Clinical Assertions: No
Region Size:20,496

Publication(s):1000 Genomes Consortium Phase 3 Integrated SV

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: 527 SVs from 71 studies. See in: genome view

Remapped(Score: Perfect):189,447,156-189,467,949

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3821564	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000001.11	Chr1	189,447,305 (-149, +50)	189,467,800 (-78, +149)
esv3821564	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000001.10	Chr1	189,416,435 (-149, +50)	189,436,930 (-78, +149)

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
essv17370026	deletion	HG00513	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,163
essv17370027	deletion	HG00566	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,182
essv17370028	deletion	HG00663	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,261
essv17370029	deletion	HG00671	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,639
essv17370030	deletion	HG00672	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,259
essv17370031	deletion	HG00689	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,593
essv17370032	deletion	HG00864	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,332
essv17370033	deletion	HG01066	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,614
essv17370034	deletion	HG01597	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,447
essv17370035	deletion	HG01796	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,389
essv17370036	deletion	HG01808	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,403
essv17370037	deletion	HG01811	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,633
essv17370038	deletion	HG01889	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,246
essv17370039	deletion	HG02113	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,108
essv17370040	deletion	HG02134	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,620
essv17370041	deletion	HG02139	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,185
essv17370042	deletion	HG02140	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,299
essv17370043	deletion	HG02367	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,628
essv17370044	deletion	HG02373	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,694
essv17370045	deletion	HG02397	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,636
essv17370046	deletion	HG02407	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,722
essv17370047	deletion	HG02582	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,147
essv17370048	deletion	HG02643	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,879
essv17370049	deletion	HG02722	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,008
essv17370050	deletion	HG02808	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,842
essv17370051	deletion	HG02810	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Homozygous	3,955
essv17370052	deletion	HG02888	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,709
essv17370053	deletion	HG03063	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,144
essv17370054	deletion	HG03190	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,090
essv17370055	deletion	HG03304	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,065
essv17370056	deletion	HG03556	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,910
essv17370057	deletion	HG03742	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,620
essv17370058	deletion	NA18486	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,705
essv17370059	deletion	NA18542	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,413
essv17370060	deletion	NA18552	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,215
essv17370061	deletion	NA18562	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,633
essv17370062	deletion	NA18954	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,085
essv17370063	deletion	NA18967	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,106
essv17370064	deletion	NA18975	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,236
essv17370065	deletion	NA18981	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,135
essv17370066	deletion	NA19002	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,182
essv17370067	deletion	NA19117	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,833
essv17370068	deletion	NA19171	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,833
essv17370069	deletion	NA19372	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	4,074
essv17370070	deletion	NA19455	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,942
essv17370071	deletion	NA19909	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,811
essv17370072	deletion	NA19917	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,589
essv17370073	deletion	NA19921	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,712
essv17370074	deletion	NA20289	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,079
essv17370075	deletion	NA20332	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,116

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv17370026	Remapped	Perfect	NC_000001.11:g.(18 9447156_189447355) _(189467722_189467 949)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	189,447,305 (-149, +50)	189,467,800 (-78, +149)
essv17370027	Remapped	Perfect	NC_000001.11:g.(18 9447156_189447355) _(189467722_189467 949)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	189,447,305 (-149, +50)	189,467,800 (-78, +149)
essv17370028	Remapped	Perfect	NC_000001.11:g.(18 9447156_189447355) _(189467722_189467 949)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	189,447,305 (-149, +50)	189,467,800 (-78, +149)
essv17370029	Remapped	Perfect	NC_000001.11:g.(18 9447156_189447355) _(189467722_189467 949)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	189,447,305 (-149, +50)	189,467,800 (-78, +149)
essv17370030	Remapped	Perfect	NC_000001.11:g.(18 9447156_189447355) _(189467722_189467 949)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	189,447,305 (-149, +50)	189,467,800 (-78, +149)
essv17370031	Remapped	Perfect	NC_000001.11:g.(18 9447156_189447355) _(189467722_189467 949)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	189,447,305 (-149, +50)	189,467,800 (-78, +149)
essv17370032	Remapped	Perfect	NC_000001.11:g.(18 9447156_189447355) _(189467722_189467 949)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	189,447,305 (-149, +50)	189,467,800 (-78, +149)
essv17370033	Remapped	Perfect	NC_000001.11:g.(18 9447156_189447355) _(189467722_189467 949)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	189,447,305 (-149, +50)	189,467,800 (-78, +149)
essv17370034	Remapped	Perfect	NC_000001.11:g.(18 9447156_189447355) _(189467722_189467 949)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	189,447,305 (-149, +50)	189,467,800 (-78, +149)
essv17370035	Remapped	Perfect	NC_000001.11:g.(18 9447156_189447355) _(189467722_189467 949)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	189,447,305 (-149, +50)	189,467,800 (-78, +149)
essv17370036	Remapped	Perfect	NC_000001.11:g.(18 9447156_189447355) _(189467722_189467 949)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	189,447,305 (-149, +50)	189,467,800 (-78, +149)
essv17370037	Remapped	Perfect	NC_000001.11:g.(18 9447156_189447355) _(189467722_189467 949)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	189,447,305 (-149, +50)	189,467,800 (-78, +149)
essv17370038	Remapped	Perfect	NC_000001.11:g.(18 9447156_189447355) _(189467722_189467 949)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	189,447,305 (-149, +50)	189,467,800 (-78, +149)
essv17370039	Remapped	Perfect	NC_000001.11:g.(18 9447156_189447355) _(189467722_189467 949)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	189,447,305 (-149, +50)	189,467,800 (-78, +149)
essv17370040	Remapped	Perfect	NC_000001.11:g.(18 9447156_189447355) _(189467722_189467 949)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	189,447,305 (-149, +50)	189,467,800 (-78, +149)
essv17370041	Remapped	Perfect	NC_000001.11:g.(18 9447156_189447355) _(189467722_189467 949)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	189,447,305 (-149, +50)	189,467,800 (-78, +149)
essv17370042	Remapped	Perfect	NC_000001.11:g.(18 9447156_189447355) _(189467722_189467 949)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	189,447,305 (-149, +50)	189,467,800 (-78, +149)
essv17370043	Remapped	Perfect	NC_000001.11:g.(18 9447156_189447355) _(189467722_189467 949)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	189,447,305 (-149, +50)	189,467,800 (-78, +149)
essv17370044	Remapped	Perfect	NC_000001.11:g.(18 9447156_189447355) _(189467722_189467 949)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	189,447,305 (-149, +50)	189,467,800 (-78, +149)
essv17370045	Remapped	Perfect	NC_000001.11:g.(18 9447156_189447355) _(189467722_189467 949)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	189,447,305 (-149, +50)	189,467,800 (-78, +149)
essv17370046	Remapped	Perfect	NC_000001.11:g.(18 9447156_189447355) _(189467722_189467 949)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	189,447,305 (-149, +50)	189,467,800 (-78, +149)
essv17370047	Remapped	Perfect	NC_000001.11:g.(18 9447156_189447355) _(189467722_189467 949)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	189,447,305 (-149, +50)	189,467,800 (-78, +149)
essv17370048	Remapped	Perfect	NC_000001.11:g.(18 9447156_189447355) _(189467722_189467 949)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	189,447,305 (-149, +50)	189,467,800 (-78, +149)
essv17370049	Remapped	Perfect	NC_000001.11:g.(18 9447156_189447355) _(189467722_189467 949)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	189,447,305 (-149, +50)	189,467,800 (-78, +149)
essv17370050	Remapped	Perfect	NC_000001.11:g.(18 9447156_189447355) _(189467722_189467 949)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	189,447,305 (-149, +50)	189,467,800 (-78, +149)
essv17370051	Remapped	Perfect	NC_000001.11:g.(18 9447156_189447355) _(189467722_189467 949)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	189,447,305 (-149, +50)	189,467,800 (-78, +149)
essv17370052	Remapped	Perfect	NC_000001.11:g.(18 9447156_189447355) _(189467722_189467 949)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	189,447,305 (-149, +50)	189,467,800 (-78, +149)
essv17370053	Remapped	Perfect	NC_000001.11:g.(18 9447156_189447355) _(189467722_189467 949)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	189,447,305 (-149, +50)	189,467,800 (-78, +149)
essv17370054	Remapped	Perfect	NC_000001.11:g.(18 9447156_189447355) _(189467722_189467 949)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	189,447,305 (-149, +50)	189,467,800 (-78, +149)
essv17370055	Remapped	Perfect	NC_000001.11:g.(18 9447156_189447355) _(189467722_189467 949)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	189,447,305 (-149, +50)	189,467,800 (-78, +149)
essv17370056	Remapped	Perfect	NC_000001.11:g.(18 9447156_189447355) _(189467722_189467 949)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	189,447,305 (-149, +50)	189,467,800 (-78, +149)
essv17370057	Remapped	Perfect	NC_000001.11:g.(18 9447156_189447355) _(189467722_189467 949)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	189,447,305 (-149, +50)	189,467,800 (-78, +149)
essv17370058	Remapped	Perfect	NC_000001.11:g.(18 9447156_189447355) _(189467722_189467 949)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	189,447,305 (-149, +50)	189,467,800 (-78, +149)
essv17370059	Remapped	Perfect	NC_000001.11:g.(18 9447156_189447355) _(189467722_189467 949)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	189,447,305 (-149, +50)	189,467,800 (-78, +149)
essv17370060	Remapped	Perfect	NC_000001.11:g.(18 9447156_189447355) _(189467722_189467 949)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	189,447,305 (-149, +50)	189,467,800 (-78, +149)
essv17370061	Remapped	Perfect	NC_000001.11:g.(18 9447156_189447355) _(189467722_189467 949)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	189,447,305 (-149, +50)	189,467,800 (-78, +149)
essv17370062	Remapped	Perfect	NC_000001.11:g.(18 9447156_189447355) _(189467722_189467 949)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	189,447,305 (-149, +50)	189,467,800 (-78, +149)
essv17370063	Remapped	Perfect	NC_000001.11:g.(18 9447156_189447355) _(189467722_189467 949)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	189,447,305 (-149, +50)	189,467,800 (-78, +149)
essv17370064	Remapped	Perfect	NC_000001.11:g.(18 9447156_189447355) _(189467722_189467 949)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	189,447,305 (-149, +50)	189,467,800 (-78, +149)
essv17370065	Remapped	Perfect	NC_000001.11:g.(18 9447156_189447355) _(189467722_189467 949)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	189,447,305 (-149, +50)	189,467,800 (-78, +149)
essv17370066	Remapped	Perfect	NC_000001.11:g.(18 9447156_189447355) _(189467722_189467 949)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	189,447,305 (-149, +50)	189,467,800 (-78, +149)
essv17370067	Remapped	Perfect	NC_000001.11:g.(18 9447156_189447355) _(189467722_189467 949)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	189,447,305 (-149, +50)	189,467,800 (-78, +149)
essv17370068	Remapped	Perfect	NC_000001.11:g.(18 9447156_189447355) _(189467722_189467 949)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	189,447,305 (-149, +50)	189,467,800 (-78, +149)
essv17370069	Remapped	Perfect	NC_000001.11:g.(18 9447156_189447355) _(189467722_189467 949)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	189,447,305 (-149, +50)	189,467,800 (-78, +149)
essv17370070	Remapped	Perfect	NC_000001.11:g.(18 9447156_189447355) _(189467722_189467 949)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	189,447,305 (-149, +50)	189,467,800 (-78, +149)
essv17370071	Remapped	Perfect	NC_000001.11:g.(18 9447156_189447355) _(189467722_189467 949)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	189,447,305 (-149, +50)	189,467,800 (-78, +149)
essv17370072	Remapped	Perfect	NC_000001.11:g.(18 9447156_189447355) _(189467722_189467 949)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	189,447,305 (-149, +50)	189,467,800 (-78, +149)
essv17370073	Remapped	Perfect	NC_000001.11:g.(18 9447156_189447355) _(189467722_189467 949)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	189,447,305 (-149, +50)	189,467,800 (-78, +149)
essv17370074	Remapped	Perfect	NC_000001.11:g.(18 9447156_189447355) _(189467722_189467 949)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	189,447,305 (-149, +50)	189,467,800 (-78, +149)
essv17370075	Remapped	Perfect	NC_000001.11:g.(18 9447156_189447355) _(189467722_189467 949)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	189,447,305 (-149, +50)	189,467,800 (-78, +149)
essv17370026	Submitted genomic		NC_000001.10:g.(18 9416286_189416485) _(189436852_189437 079)del	GRCh37 (hg19)		NC_000001.10	Chr1	189,416,435 (-149, +50)	189,436,930 (-78, +149)
essv17370027	Submitted genomic		NC_000001.10:g.(18 9416286_189416485) _(189436852_189437 079)del	GRCh37 (hg19)		NC_000001.10	Chr1	189,416,435 (-149, +50)	189,436,930 (-78, +149)
essv17370028	Submitted genomic		NC_000001.10:g.(18 9416286_189416485) _(189436852_189437 079)del	GRCh37 (hg19)		NC_000001.10	Chr1	189,416,435 (-149, +50)	189,436,930 (-78, +149)
essv17370029	Submitted genomic		NC_000001.10:g.(18 9416286_189416485) _(189436852_189437 079)del	GRCh37 (hg19)		NC_000001.10	Chr1	189,416,435 (-149, +50)	189,436,930 (-78, +149)
essv17370030	Submitted genomic		NC_000001.10:g.(18 9416286_189416485) _(189436852_189437 079)del	GRCh37 (hg19)		NC_000001.10	Chr1	189,416,435 (-149, +50)	189,436,930 (-78, +149)
essv17370031	Submitted genomic		NC_000001.10:g.(18 9416286_189416485) _(189436852_189437 079)del	GRCh37 (hg19)		NC_000001.10	Chr1	189,416,435 (-149, +50)	189,436,930 (-78, +149)
essv17370032	Submitted genomic		NC_000001.10:g.(18 9416286_189416485) _(189436852_189437 079)del	GRCh37 (hg19)		NC_000001.10	Chr1	189,416,435 (-149, +50)	189,436,930 (-78, +149)
essv17370033	Submitted genomic		NC_000001.10:g.(18 9416286_189416485) _(189436852_189437 079)del	GRCh37 (hg19)		NC_000001.10	Chr1	189,416,435 (-149, +50)	189,436,930 (-78, +149)
essv17370034	Submitted genomic		NC_000001.10:g.(18 9416286_189416485) _(189436852_189437 079)del	GRCh37 (hg19)		NC_000001.10	Chr1	189,416,435 (-149, +50)	189,436,930 (-78, +149)
essv17370035	Submitted genomic		NC_000001.10:g.(18 9416286_189416485) _(189436852_189437 079)del	GRCh37 (hg19)		NC_000001.10	Chr1	189,416,435 (-149, +50)	189,436,930 (-78, +149)
essv17370036	Submitted genomic		NC_000001.10:g.(18 9416286_189416485) _(189436852_189437 079)del	GRCh37 (hg19)		NC_000001.10	Chr1	189,416,435 (-149, +50)	189,436,930 (-78, +149)
essv17370037	Submitted genomic		NC_000001.10:g.(18 9416286_189416485) _(189436852_189437 079)del	GRCh37 (hg19)		NC_000001.10	Chr1	189,416,435 (-149, +50)	189,436,930 (-78, +149)
essv17370038	Submitted genomic		NC_000001.10:g.(18 9416286_189416485) _(189436852_189437 079)del	GRCh37 (hg19)		NC_000001.10	Chr1	189,416,435 (-149, +50)	189,436,930 (-78, +149)
essv17370039	Submitted genomic		NC_000001.10:g.(18 9416286_189416485) _(189436852_189437 079)del	GRCh37 (hg19)		NC_000001.10	Chr1	189,416,435 (-149, +50)	189,436,930 (-78, +149)
essv17370040	Submitted genomic		NC_000001.10:g.(18 9416286_189416485) _(189436852_189437 079)del	GRCh37 (hg19)		NC_000001.10	Chr1	189,416,435 (-149, +50)	189,436,930 (-78, +149)
essv17370041	Submitted genomic		NC_000001.10:g.(18 9416286_189416485) _(189436852_189437 079)del	GRCh37 (hg19)		NC_000001.10	Chr1	189,416,435 (-149, +50)	189,436,930 (-78, +149)
essv17370042	Submitted genomic		NC_000001.10:g.(18 9416286_189416485) _(189436852_189437 079)del	GRCh37 (hg19)		NC_000001.10	Chr1	189,416,435 (-149, +50)	189,436,930 (-78, +149)
essv17370043	Submitted genomic		NC_000001.10:g.(18 9416286_189416485) _(189436852_189437 079)del	GRCh37 (hg19)		NC_000001.10	Chr1	189,416,435 (-149, +50)	189,436,930 (-78, +149)
essv17370044	Submitted genomic		NC_000001.10:g.(18 9416286_189416485) _(189436852_189437 079)del	GRCh37 (hg19)		NC_000001.10	Chr1	189,416,435 (-149, +50)	189,436,930 (-78, +149)
essv17370045	Submitted genomic		NC_000001.10:g.(18 9416286_189416485) _(189436852_189437 079)del	GRCh37 (hg19)		NC_000001.10	Chr1	189,416,435 (-149, +50)	189,436,930 (-78, +149)
essv17370046	Submitted genomic		NC_000001.10:g.(18 9416286_189416485) _(189436852_189437 079)del	GRCh37 (hg19)		NC_000001.10	Chr1	189,416,435 (-149, +50)	189,436,930 (-78, +149)
essv17370047	Submitted genomic		NC_000001.10:g.(18 9416286_189416485) _(189436852_189437 079)del	GRCh37 (hg19)		NC_000001.10	Chr1	189,416,435 (-149, +50)	189,436,930 (-78, +149)
essv17370048	Submitted genomic		NC_000001.10:g.(18 9416286_189416485) _(189436852_189437 079)del	GRCh37 (hg19)		NC_000001.10	Chr1	189,416,435 (-149, +50)	189,436,930 (-78, +149)
essv17370049	Submitted genomic		NC_000001.10:g.(18 9416286_189416485) _(189436852_189437 079)del	GRCh37 (hg19)		NC_000001.10	Chr1	189,416,435 (-149, +50)	189,436,930 (-78, +149)
essv17370050	Submitted genomic		NC_000001.10:g.(18 9416286_189416485) _(189436852_189437 079)del	GRCh37 (hg19)		NC_000001.10	Chr1	189,416,435 (-149, +50)	189,436,930 (-78, +149)
essv17370051	Submitted genomic		NC_000001.10:g.(18 9416286_189416485) _(189436852_189437 079)del	GRCh37 (hg19)		NC_000001.10	Chr1	189,416,435 (-149, +50)	189,436,930 (-78, +149)
essv17370052	Submitted genomic		NC_000001.10:g.(18 9416286_189416485) _(189436852_189437 079)del	GRCh37 (hg19)		NC_000001.10	Chr1	189,416,435 (-149, +50)	189,436,930 (-78, +149)
essv17370053	Submitted genomic		NC_000001.10:g.(18 9416286_189416485) _(189436852_189437 079)del	GRCh37 (hg19)		NC_000001.10	Chr1	189,416,435 (-149, +50)	189,436,930 (-78, +149)
essv17370054	Submitted genomic		NC_000001.10:g.(18 9416286_189416485) _(189436852_189437 079)del	GRCh37 (hg19)		NC_000001.10	Chr1	189,416,435 (-149, +50)	189,436,930 (-78, +149)
essv17370055	Submitted genomic		NC_000001.10:g.(18 9416286_189416485) _(189436852_189437 079)del	GRCh37 (hg19)		NC_000001.10	Chr1	189,416,435 (-149, +50)	189,436,930 (-78, +149)
essv17370056	Submitted genomic		NC_000001.10:g.(18 9416286_189416485) _(189436852_189437 079)del	GRCh37 (hg19)		NC_000001.10	Chr1	189,416,435 (-149, +50)	189,436,930 (-78, +149)
essv17370057	Submitted genomic		NC_000001.10:g.(18 9416286_189416485) _(189436852_189437 079)del	GRCh37 (hg19)		NC_000001.10	Chr1	189,416,435 (-149, +50)	189,436,930 (-78, +149)
essv17370058	Submitted genomic		NC_000001.10:g.(18 9416286_189416485) _(189436852_189437 079)del	GRCh37 (hg19)		NC_000001.10	Chr1	189,416,435 (-149, +50)	189,436,930 (-78, +149)
essv17370059	Submitted genomic		NC_000001.10:g.(18 9416286_189416485) _(189436852_189437 079)del	GRCh37 (hg19)		NC_000001.10	Chr1	189,416,435 (-149, +50)	189,436,930 (-78, +149)
essv17370060	Submitted genomic		NC_000001.10:g.(18 9416286_189416485) _(189436852_189437 079)del	GRCh37 (hg19)		NC_000001.10	Chr1	189,416,435 (-149, +50)	189,436,930 (-78, +149)
essv17370061	Submitted genomic		NC_000001.10:g.(18 9416286_189416485) _(189436852_189437 079)del	GRCh37 (hg19)		NC_000001.10	Chr1	189,416,435 (-149, +50)	189,436,930 (-78, +149)
essv17370062	Submitted genomic		NC_000001.10:g.(18 9416286_189416485) _(189436852_189437 079)del	GRCh37 (hg19)		NC_000001.10	Chr1	189,416,435 (-149, +50)	189,436,930 (-78, +149)
essv17370063	Submitted genomic		NC_000001.10:g.(18 9416286_189416485) _(189436852_189437 079)del	GRCh37 (hg19)		NC_000001.10	Chr1	189,416,435 (-149, +50)	189,436,930 (-78, +149)
essv17370064	Submitted genomic		NC_000001.10:g.(18 9416286_189416485) _(189436852_189437 079)del	GRCh37 (hg19)		NC_000001.10	Chr1	189,416,435 (-149, +50)	189,436,930 (-78, +149)
essv17370065	Submitted genomic		NC_000001.10:g.(18 9416286_189416485) _(189436852_189437 079)del	GRCh37 (hg19)		NC_000001.10	Chr1	189,416,435 (-149, +50)	189,436,930 (-78, +149)
essv17370066	Submitted genomic		NC_000001.10:g.(18 9416286_189416485) _(189436852_189437 079)del	GRCh37 (hg19)		NC_000001.10	Chr1	189,416,435 (-149, +50)	189,436,930 (-78, +149)
essv17370067	Submitted genomic		NC_000001.10:g.(18 9416286_189416485) _(189436852_189437 079)del	GRCh37 (hg19)		NC_000001.10	Chr1	189,416,435 (-149, +50)	189,436,930 (-78, +149)
essv17370068	Submitted genomic		NC_000001.10:g.(18 9416286_189416485) _(189436852_189437 079)del	GRCh37 (hg19)		NC_000001.10	Chr1	189,416,435 (-149, +50)	189,436,930 (-78, +149)
essv17370069	Submitted genomic		NC_000001.10:g.(18 9416286_189416485) _(189436852_189437 079)del	GRCh37 (hg19)		NC_000001.10	Chr1	189,416,435 (-149, +50)	189,436,930 (-78, +149)
essv17370070	Submitted genomic		NC_000001.10:g.(18 9416286_189416485) _(189436852_189437 079)del	GRCh37 (hg19)		NC_000001.10	Chr1	189,416,435 (-149, +50)	189,436,930 (-78, +149)
essv17370071	Submitted genomic		NC_000001.10:g.(18 9416286_189416485) _(189436852_189437 079)del	GRCh37 (hg19)		NC_000001.10	Chr1	189,416,435 (-149, +50)	189,436,930 (-78, +149)
essv17370072	Submitted genomic		NC_000001.10:g.(18 9416286_189416485) _(189436852_189437 079)del	GRCh37 (hg19)		NC_000001.10	Chr1	189,416,435 (-149, +50)	189,436,930 (-78, +149)
essv17370073	Submitted genomic		NC_000001.10:g.(18 9416286_189416485) _(189436852_189437 079)del	GRCh37 (hg19)		NC_000001.10	Chr1	189,416,435 (-149, +50)	189,436,930 (-78, +149)
essv17370074	Submitted genomic		NC_000001.10:g.(18 9416286_189416485) _(189436852_189437 079)del	GRCh37 (hg19)		NC_000001.10	Chr1	189,416,435 (-149, +50)	189,436,930 (-78, +149)
essv17370075	Submitted genomic		NC_000001.10:g.(18 9416286_189416485) _(189436852_189437 079)del	GRCh37 (hg19)		NC_000001.10	Chr1	189,416,435 (-149, +50)	189,436,930 (-78, +149)

dbVar

Database of genomic structural variation

esv3821564

Links to Other Resources

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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.