esv3855790

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:69
Validation:Not tested
Clinical Assertions: No
Region Size:182,091

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: 1371 SVs from 94 studies. See in: genome view

Remapped(Score: Perfect):136,668,040-136,850,131

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3855790	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
esv3855790	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000008.10	Chr8	137,680,283 (-0, +1)	137,862,373 (-0, +1)

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
essv21392776	deletion	HG00131	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,620
essv21392777	deletion	HG00327	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	2,997
essv21392778	deletion	HG00338	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,371
essv21392779	deletion	HG01080	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,389
essv21392780	deletion	HG01275	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,017
essv21392781	deletion	HG01350	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,558
essv21392782	deletion	HG01359	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,531
essv21392783	deletion	HG01465	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,250
essv21392784	deletion	HG01522	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,227
essv21392785	deletion	HG01550	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,113
essv21392786	deletion	HG02601	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,373
essv21392787	deletion	HG02603	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,537
essv21392788	deletion	HG02648	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,681
essv21392789	deletion	HG02657	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,652
essv21392790	deletion	HG02691	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,484
essv21392791	deletion	HG02793	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,464
essv21392792	deletion	HG03238	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,441
essv21392793	deletion	HG03652	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,127
essv21392794	deletion	HG03668	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,475
essv21392795	deletion	HG03703	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,411
essv21392796	deletion	HG03717	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,367
essv21392797	deletion	HG03718	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Homozygous	3,516
essv21392798	deletion	HG03729	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,673
essv21392799	deletion	HG03740	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,604
essv21392800	deletion	HG03779	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,644
essv21392801	deletion	HG03785	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,488
essv21392802	deletion	HG03790	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,521
essv21392803	deletion	HG03848	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,539
essv21392804	deletion	HG03849	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,475
essv21392805	deletion	HG03861	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,223
essv21392806	deletion	HG03863	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,227
essv21392807	deletion	HG03896	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,613
essv21392808	deletion	HG03914	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,435
essv21392809	deletion	HG03917	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,709
essv21392810	deletion	HG03928	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,278
essv21392811	deletion	HG03960	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,441
essv21392812	deletion	HG03998	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,159
essv21392813	deletion	HG04001	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	2,913
essv21392814	deletion	HG04023	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,089
essv21392815	deletion	HG04025	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,135
essv21392816	deletion	HG04026	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,157
essv21392817	deletion	HG04042	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,018
essv21392818	deletion	HG04054	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	2,819
essv21392819	deletion	HG04056	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,093
essv21392820	deletion	HG04063	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,140
essv21392821	deletion	HG04098	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,738
essv21392822	deletion	HG04171	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,431
essv21392823	deletion	HG04194	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,673
essv21392824	deletion	HG04214	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,517
essv21392825	deletion	NA07357	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,777
essv21392826	deletion	NA11832	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,358
essv21392827	deletion	NA12249	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	2,981
essv21392828	deletion	NA12775	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,650
essv21392829	deletion	NA12874	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,371
essv21392830	deletion	NA19663	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,103
essv21392831	deletion	NA20509	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Homozygous	3,757
essv21392832	deletion	NA20511	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,587
essv21392833	deletion	NA20524	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,634
essv21392834	deletion	NA20543	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,670
essv21392835	deletion	NA20753	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,496
essv21392836	deletion	NA20778	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,698
essv21392837	deletion	NA20800	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,274
essv21392838	deletion	NA20849	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,504
essv21392839	deletion	NA20864	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,644
essv21392840	deletion	NA20877	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,335
essv21392841	deletion	NA20890	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,378
essv21392842	deletion	NA21090	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,178
essv21392843	deletion	NA21126	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,574
essv21392844	deletion	NA21130	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,714

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv21392776	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392777	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392778	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392779	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392780	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392781	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392782	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392783	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392784	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392785	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392786	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392787	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392788	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392789	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392790	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392791	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392792	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392793	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392794	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392795	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392796	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392797	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392798	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392799	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392800	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392801	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392802	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392803	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392804	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392805	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392806	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392807	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392808	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392809	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392810	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392811	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392812	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392813	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392814	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392815	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392816	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392817	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392818	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392819	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392820	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392821	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392822	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392823	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392824	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392825	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392826	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392827	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392828	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392829	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392830	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392831	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392832	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392833	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392834	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392835	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392836	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392837	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392838	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392839	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392840	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392841	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392842	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392843	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392844	Remapped	Perfect	NC_000008.11:g.(13 6668040_136668041) _(136850130_136850 131)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	136,668,040 (-0, +1)	136,850,130 (-0, +1)
essv21392776	Submitted genomic		NC_000008.10:g.(13 7680283_137680284) _(137862373_137862 374)del	GRCh37 (hg19)		NC_000008.10	Chr8	137,680,283 (-0, +1)	137,862,373 (-0, +1)
essv21392777	Submitted genomic		NC_000008.10:g.(13 7680283_137680284) _(137862373_137862 374)del	GRCh37 (hg19)		NC_000008.10	Chr8	137,680,283 (-0, +1)	137,862,373 (-0, +1)
essv21392778	Submitted genomic		NC_000008.10:g.(13 7680283_137680284) _(137862373_137862 374)del	GRCh37 (hg19)		NC_000008.10	Chr8	137,680,283 (-0, +1)	137,862,373 (-0, +1)
essv21392779	Submitted genomic		NC_000008.10:g.(13 7680283_137680284) _(137862373_137862 374)del	GRCh37 (hg19)		NC_000008.10	Chr8	137,680,283 (-0, +1)	137,862,373 (-0, +1)
essv21392780	Submitted genomic		NC_000008.10:g.(13 7680283_137680284) _(137862373_137862 374)del	GRCh37 (hg19)		NC_000008.10	Chr8	137,680,283 (-0, +1)	137,862,373 (-0, +1)
essv21392781	Submitted genomic		NC_000008.10:g.(13 7680283_137680284) _(137862373_137862 374)del	GRCh37 (hg19)		NC_000008.10	Chr8	137,680,283 (-0, +1)	137,862,373 (-0, +1)
essv21392782	Submitted genomic		NC_000008.10:g.(13 7680283_137680284) _(137862373_137862 374)del	GRCh37 (hg19)		NC_000008.10	Chr8	137,680,283 (-0, +1)	137,862,373 (-0, +1)
essv21392783	Submitted genomic		NC_000008.10:g.(13 7680283_137680284) _(137862373_137862 374)del	GRCh37 (hg19)		NC_000008.10	Chr8	137,680,283 (-0, +1)	137,862,373 (-0, +1)
essv21392784	Submitted genomic		NC_000008.10:g.(13 7680283_137680284) _(137862373_137862 374)del	GRCh37 (hg19)		NC_000008.10	Chr8	137,680,283 (-0, +1)	137,862,373 (-0, +1)
essv21392785	Submitted genomic		NC_000008.10:g.(13 7680283_137680284) _(137862373_137862 374)del	GRCh37 (hg19)		NC_000008.10	Chr8	137,680,283 (-0, +1)	137,862,373 (-0, +1)
essv21392786	Submitted genomic		NC_000008.10:g.(13 7680283_137680284) _(137862373_137862 374)del	GRCh37 (hg19)		NC_000008.10	Chr8	137,680,283 (-0, +1)	137,862,373 (-0, +1)
essv21392787	Submitted genomic		NC_000008.10:g.(13 7680283_137680284) _(137862373_137862 374)del	GRCh37 (hg19)		NC_000008.10	Chr8	137,680,283 (-0, +1)	137,862,373 (-0, +1)
essv21392788	Submitted genomic		NC_000008.10:g.(13 7680283_137680284) _(137862373_137862 374)del	GRCh37 (hg19)		NC_000008.10	Chr8	137,680,283 (-0, +1)	137,862,373 (-0, +1)
essv21392789	Submitted genomic		NC_000008.10:g.(13 7680283_137680284) _(137862373_137862 374)del	GRCh37 (hg19)		NC_000008.10	Chr8	137,680,283 (-0, +1)	137,862,373 (-0, +1)
essv21392790	Submitted genomic		NC_000008.10:g.(13 7680283_137680284) _(137862373_137862 374)del	GRCh37 (hg19)		NC_000008.10	Chr8	137,680,283 (-0, +1)	137,862,373 (-0, +1)
essv21392791	Submitted genomic		NC_000008.10:g.(13 7680283_137680284) _(137862373_137862 374)del	GRCh37 (hg19)		NC_000008.10	Chr8	137,680,283 (-0, +1)	137,862,373 (-0, +1)
essv21392792	Submitted genomic		NC_000008.10:g.(13 7680283_137680284) _(137862373_137862 374)del	GRCh37 (hg19)		NC_000008.10	Chr8	137,680,283 (-0, +1)	137,862,373 (-0, +1)
essv21392793	Submitted genomic		NC_000008.10:g.(13 7680283_137680284) _(137862373_137862 374)del	GRCh37 (hg19)		NC_000008.10	Chr8	137,680,283 (-0, +1)	137,862,373 (-0, +1)
essv21392794	Submitted genomic		NC_000008.10:g.(13 7680283_137680284) _(137862373_137862 374)del	GRCh37 (hg19)		NC_000008.10	Chr8	137,680,283 (-0, +1)	137,862,373 (-0, +1)
essv21392795	Submitted genomic		NC_000008.10:g.(13 7680283_137680284) _(137862373_137862 374)del	GRCh37 (hg19)		NC_000008.10	Chr8	137,680,283 (-0, +1)	137,862,373 (-0, +1)
essv21392796	Submitted genomic		NC_000008.10:g.(13 7680283_137680284) _(137862373_137862 374)del	GRCh37 (hg19)		NC_000008.10	Chr8	137,680,283 (-0, +1)	137,862,373 (-0, +1)
essv21392797	Submitted genomic		NC_000008.10:g.(13 7680283_137680284) _(137862373_137862 374)del	GRCh37 (hg19)		NC_000008.10	Chr8	137,680,283 (-0, +1)	137,862,373 (-0, +1)
essv21392798	Submitted genomic		NC_000008.10:g.(13 7680283_137680284) _(137862373_137862 374)del	GRCh37 (hg19)		NC_000008.10	Chr8	137,680,283 (-0, +1)	137,862,373 (-0, +1)
essv21392799	Submitted genomic		NC_000008.10:g.(13 7680283_137680284) _(137862373_137862 374)del	GRCh37 (hg19)		NC_000008.10	Chr8	137,680,283 (-0, +1)	137,862,373 (-0, +1)
essv21392800	Submitted genomic		NC_000008.10:g.(13 7680283_137680284) _(137862373_137862 374)del	GRCh37 (hg19)		NC_000008.10	Chr8	137,680,283 (-0, +1)	137,862,373 (-0, +1)
essv21392801	Submitted genomic		NC_000008.10:g.(13 7680283_137680284) _(137862373_137862 374)del	GRCh37 (hg19)		NC_000008.10	Chr8	137,680,283 (-0, +1)	137,862,373 (-0, +1)
essv21392802	Submitted genomic		NC_000008.10:g.(13 7680283_137680284) _(137862373_137862 374)del	GRCh37 (hg19)		NC_000008.10	Chr8	137,680,283 (-0, +1)	137,862,373 (-0, +1)
essv21392803	Submitted genomic		NC_000008.10:g.(13 7680283_137680284) _(137862373_137862 374)del	GRCh37 (hg19)		NC_000008.10	Chr8	137,680,283 (-0, +1)	137,862,373 (-0, +1)
essv21392804	Submitted genomic		NC_000008.10:g.(13 7680283_137680284) _(137862373_137862 374)del	GRCh37 (hg19)		NC_000008.10	Chr8	137,680,283 (-0, +1)	137,862,373 (-0, +1)
essv21392805	Submitted genomic		NC_000008.10:g.(13 7680283_137680284) _(137862373_137862 374)del	GRCh37 (hg19)		NC_000008.10	Chr8	137,680,283 (-0, +1)	137,862,373 (-0, +1)
essv21392806	Submitted genomic		NC_000008.10:g.(13 7680283_137680284) _(137862373_137862 374)del	GRCh37 (hg19)		NC_000008.10	Chr8	137,680,283 (-0, +1)	137,862,373 (-0, +1)

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dbVar

Database of genomic structural variation

esv3855790

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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.