esv3865261

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:38
Validation:Not tested
Clinical Assertions: No
Region Size:12,402

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: 210 SVs from 47 studies. See in: genome view

Remapped(Score: Perfect):99,775,318-99,789,719

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3865261	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000011.10	Chr11	99,776,318 (-1000, +500)	99,788,719 (-500, +1000)
esv3865261	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000011.9	Chr11	99,647,049 (-1000, +500)	99,659,450 (-500, +1000)

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
essv22543235	deletion	HG00406	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,569
essv22543236	deletion	HG00409	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,535
essv22543237	deletion	HG00475	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,651
essv22543238	deletion	HG00537	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,132
essv22543239	deletion	HG00542	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,469
essv22543240	deletion	HG00565	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,548
essv22543241	deletion	HG00607	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,540
essv22543242	deletion	HG00613	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,613
essv22543243	deletion	HG00759	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,479
essv22543244	deletion	HG00881	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,669
essv22543245	deletion	HG01804	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,402
essv22543246	deletion	HG01857	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,273
essv22543247	deletion	HG01933	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,343
essv22543248	deletion	HG02017	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,737
essv22543249	deletion	HG02029	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,514
essv22543250	deletion	HG02079	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,664
essv22543251	deletion	HG02087	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,212
essv22543252	deletion	HG02375	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,654
essv22543253	deletion	HG02398	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,696
essv22543254	deletion	HG02513	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,363
essv22543255	deletion	HG04195	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,469
essv22543256	deletion	NA18546	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,615
essv22543257	deletion	NA18557	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,575
essv22543258	deletion	NA18559	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,544
essv22543259	deletion	NA18599	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,511
essv22543260	deletion	NA18605	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,715
essv22543261	deletion	NA18623	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,604
essv22543262	deletion	NA18632	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,578
essv22543263	deletion	NA18644	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	2,754
essv22543264	deletion	NA18943	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,734
essv22543265	deletion	NA18950	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,551
essv22543266	deletion	NA18954	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,085
essv22543267	deletion	NA18975	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,236
essv22543268	deletion	NA18993	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,206
essv22543269	deletion	NA18995	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,441
essv22543270	deletion	NA19012	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,569
essv22543271	deletion	NA19058	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,502
essv22543272	deletion	NA19083	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,398

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv22543235	Remapped	Perfect	NC_000011.10:g.(99 775318_99776818)_( 99788219_99789719) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	99,776,318 (-1000, +500)	99,788,719 (-500, +1000)
essv22543236	Remapped	Perfect	NC_000011.10:g.(99 775318_99776818)_( 99788219_99789719) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	99,776,318 (-1000, +500)	99,788,719 (-500, +1000)
essv22543237	Remapped	Perfect	NC_000011.10:g.(99 775318_99776818)_( 99788219_99789719) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	99,776,318 (-1000, +500)	99,788,719 (-500, +1000)
essv22543238	Remapped	Perfect	NC_000011.10:g.(99 775318_99776818)_( 99788219_99789719) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	99,776,318 (-1000, +500)	99,788,719 (-500, +1000)
essv22543239	Remapped	Perfect	NC_000011.10:g.(99 775318_99776818)_( 99788219_99789719) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	99,776,318 (-1000, +500)	99,788,719 (-500, +1000)
essv22543240	Remapped	Perfect	NC_000011.10:g.(99 775318_99776818)_( 99788219_99789719) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	99,776,318 (-1000, +500)	99,788,719 (-500, +1000)
essv22543241	Remapped	Perfect	NC_000011.10:g.(99 775318_99776818)_( 99788219_99789719) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	99,776,318 (-1000, +500)	99,788,719 (-500, +1000)
essv22543242	Remapped	Perfect	NC_000011.10:g.(99 775318_99776818)_( 99788219_99789719) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	99,776,318 (-1000, +500)	99,788,719 (-500, +1000)
essv22543243	Remapped	Perfect	NC_000011.10:g.(99 775318_99776818)_( 99788219_99789719) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	99,776,318 (-1000, +500)	99,788,719 (-500, +1000)
essv22543244	Remapped	Perfect	NC_000011.10:g.(99 775318_99776818)_( 99788219_99789719) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	99,776,318 (-1000, +500)	99,788,719 (-500, +1000)
essv22543245	Remapped	Perfect	NC_000011.10:g.(99 775318_99776818)_( 99788219_99789719) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	99,776,318 (-1000, +500)	99,788,719 (-500, +1000)
essv22543246	Remapped	Perfect	NC_000011.10:g.(99 775318_99776818)_( 99788219_99789719) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	99,776,318 (-1000, +500)	99,788,719 (-500, +1000)
essv22543247	Remapped	Perfect	NC_000011.10:g.(99 775318_99776818)_( 99788219_99789719) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	99,776,318 (-1000, +500)	99,788,719 (-500, +1000)
essv22543248	Remapped	Perfect	NC_000011.10:g.(99 775318_99776818)_( 99788219_99789719) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	99,776,318 (-1000, +500)	99,788,719 (-500, +1000)
essv22543249	Remapped	Perfect	NC_000011.10:g.(99 775318_99776818)_( 99788219_99789719) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	99,776,318 (-1000, +500)	99,788,719 (-500, +1000)
essv22543250	Remapped	Perfect	NC_000011.10:g.(99 775318_99776818)_( 99788219_99789719) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	99,776,318 (-1000, +500)	99,788,719 (-500, +1000)
essv22543251	Remapped	Perfect	NC_000011.10:g.(99 775318_99776818)_( 99788219_99789719) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	99,776,318 (-1000, +500)	99,788,719 (-500, +1000)
essv22543252	Remapped	Perfect	NC_000011.10:g.(99 775318_99776818)_( 99788219_99789719) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	99,776,318 (-1000, +500)	99,788,719 (-500, +1000)
essv22543253	Remapped	Perfect	NC_000011.10:g.(99 775318_99776818)_( 99788219_99789719) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	99,776,318 (-1000, +500)	99,788,719 (-500, +1000)
essv22543254	Remapped	Perfect	NC_000011.10:g.(99 775318_99776818)_( 99788219_99789719) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	99,776,318 (-1000, +500)	99,788,719 (-500, +1000)
essv22543255	Remapped	Perfect	NC_000011.10:g.(99 775318_99776818)_( 99788219_99789719) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	99,776,318 (-1000, +500)	99,788,719 (-500, +1000)
essv22543256	Remapped	Perfect	NC_000011.10:g.(99 775318_99776818)_( 99788219_99789719) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	99,776,318 (-1000, +500)	99,788,719 (-500, +1000)
essv22543257	Remapped	Perfect	NC_000011.10:g.(99 775318_99776818)_( 99788219_99789719) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	99,776,318 (-1000, +500)	99,788,719 (-500, +1000)
essv22543258	Remapped	Perfect	NC_000011.10:g.(99 775318_99776818)_( 99788219_99789719) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	99,776,318 (-1000, +500)	99,788,719 (-500, +1000)
essv22543259	Remapped	Perfect	NC_000011.10:g.(99 775318_99776818)_( 99788219_99789719) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	99,776,318 (-1000, +500)	99,788,719 (-500, +1000)
essv22543260	Remapped	Perfect	NC_000011.10:g.(99 775318_99776818)_( 99788219_99789719) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	99,776,318 (-1000, +500)	99,788,719 (-500, +1000)
essv22543261	Remapped	Perfect	NC_000011.10:g.(99 775318_99776818)_( 99788219_99789719) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	99,776,318 (-1000, +500)	99,788,719 (-500, +1000)
essv22543262	Remapped	Perfect	NC_000011.10:g.(99 775318_99776818)_( 99788219_99789719) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	99,776,318 (-1000, +500)	99,788,719 (-500, +1000)
essv22543263	Remapped	Perfect	NC_000011.10:g.(99 775318_99776818)_( 99788219_99789719) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	99,776,318 (-1000, +500)	99,788,719 (-500, +1000)
essv22543264	Remapped	Perfect	NC_000011.10:g.(99 775318_99776818)_( 99788219_99789719) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	99,776,318 (-1000, +500)	99,788,719 (-500, +1000)
essv22543265	Remapped	Perfect	NC_000011.10:g.(99 775318_99776818)_( 99788219_99789719) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	99,776,318 (-1000, +500)	99,788,719 (-500, +1000)
essv22543266	Remapped	Perfect	NC_000011.10:g.(99 775318_99776818)_( 99788219_99789719) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	99,776,318 (-1000, +500)	99,788,719 (-500, +1000)
essv22543267	Remapped	Perfect	NC_000011.10:g.(99 775318_99776818)_( 99788219_99789719) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	99,776,318 (-1000, +500)	99,788,719 (-500, +1000)
essv22543268	Remapped	Perfect	NC_000011.10:g.(99 775318_99776818)_( 99788219_99789719) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	99,776,318 (-1000, +500)	99,788,719 (-500, +1000)
essv22543269	Remapped	Perfect	NC_000011.10:g.(99 775318_99776818)_( 99788219_99789719) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	99,776,318 (-1000, +500)	99,788,719 (-500, +1000)
essv22543270	Remapped	Perfect	NC_000011.10:g.(99 775318_99776818)_( 99788219_99789719) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	99,776,318 (-1000, +500)	99,788,719 (-500, +1000)
essv22543271	Remapped	Perfect	NC_000011.10:g.(99 775318_99776818)_( 99788219_99789719) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	99,776,318 (-1000, +500)	99,788,719 (-500, +1000)
essv22543272	Remapped	Perfect	NC_000011.10:g.(99 775318_99776818)_( 99788219_99789719) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	99,776,318 (-1000, +500)	99,788,719 (-500, +1000)
essv22543235	Submitted genomic		NC_000011.9:g.(996 46049_99647549)_(9 9658950_99660450)d el	GRCh37 (hg19)		NC_000011.9	Chr11	99,647,049 (-1000, +500)	99,659,450 (-500, +1000)
essv22543236	Submitted genomic		NC_000011.9:g.(996 46049_99647549)_(9 9658950_99660450)d el	GRCh37 (hg19)		NC_000011.9	Chr11	99,647,049 (-1000, +500)	99,659,450 (-500, +1000)
essv22543237	Submitted genomic		NC_000011.9:g.(996 46049_99647549)_(9 9658950_99660450)d el	GRCh37 (hg19)		NC_000011.9	Chr11	99,647,049 (-1000, +500)	99,659,450 (-500, +1000)
essv22543238	Submitted genomic		NC_000011.9:g.(996 46049_99647549)_(9 9658950_99660450)d el	GRCh37 (hg19)		NC_000011.9	Chr11	99,647,049 (-1000, +500)	99,659,450 (-500, +1000)
essv22543239	Submitted genomic		NC_000011.9:g.(996 46049_99647549)_(9 9658950_99660450)d el	GRCh37 (hg19)		NC_000011.9	Chr11	99,647,049 (-1000, +500)	99,659,450 (-500, +1000)
essv22543240	Submitted genomic		NC_000011.9:g.(996 46049_99647549)_(9 9658950_99660450)d el	GRCh37 (hg19)		NC_000011.9	Chr11	99,647,049 (-1000, +500)	99,659,450 (-500, +1000)
essv22543241	Submitted genomic		NC_000011.9:g.(996 46049_99647549)_(9 9658950_99660450)d el	GRCh37 (hg19)		NC_000011.9	Chr11	99,647,049 (-1000, +500)	99,659,450 (-500, +1000)
essv22543242	Submitted genomic		NC_000011.9:g.(996 46049_99647549)_(9 9658950_99660450)d el	GRCh37 (hg19)		NC_000011.9	Chr11	99,647,049 (-1000, +500)	99,659,450 (-500, +1000)
essv22543243	Submitted genomic		NC_000011.9:g.(996 46049_99647549)_(9 9658950_99660450)d el	GRCh37 (hg19)		NC_000011.9	Chr11	99,647,049 (-1000, +500)	99,659,450 (-500, +1000)
essv22543244	Submitted genomic		NC_000011.9:g.(996 46049_99647549)_(9 9658950_99660450)d el	GRCh37 (hg19)		NC_000011.9	Chr11	99,647,049 (-1000, +500)	99,659,450 (-500, +1000)
essv22543245	Submitted genomic		NC_000011.9:g.(996 46049_99647549)_(9 9658950_99660450)d el	GRCh37 (hg19)		NC_000011.9	Chr11	99,647,049 (-1000, +500)	99,659,450 (-500, +1000)
essv22543246	Submitted genomic		NC_000011.9:g.(996 46049_99647549)_(9 9658950_99660450)d el	GRCh37 (hg19)		NC_000011.9	Chr11	99,647,049 (-1000, +500)	99,659,450 (-500, +1000)
essv22543247	Submitted genomic		NC_000011.9:g.(996 46049_99647549)_(9 9658950_99660450)d el	GRCh37 (hg19)		NC_000011.9	Chr11	99,647,049 (-1000, +500)	99,659,450 (-500, +1000)
essv22543248	Submitted genomic		NC_000011.9:g.(996 46049_99647549)_(9 9658950_99660450)d el	GRCh37 (hg19)		NC_000011.9	Chr11	99,647,049 (-1000, +500)	99,659,450 (-500, +1000)
essv22543249	Submitted genomic		NC_000011.9:g.(996 46049_99647549)_(9 9658950_99660450)d el	GRCh37 (hg19)		NC_000011.9	Chr11	99,647,049 (-1000, +500)	99,659,450 (-500, +1000)
essv22543250	Submitted genomic		NC_000011.9:g.(996 46049_99647549)_(9 9658950_99660450)d el	GRCh37 (hg19)		NC_000011.9	Chr11	99,647,049 (-1000, +500)	99,659,450 (-500, +1000)
essv22543251	Submitted genomic		NC_000011.9:g.(996 46049_99647549)_(9 9658950_99660450)d el	GRCh37 (hg19)		NC_000011.9	Chr11	99,647,049 (-1000, +500)	99,659,450 (-500, +1000)
essv22543252	Submitted genomic		NC_000011.9:g.(996 46049_99647549)_(9 9658950_99660450)d el	GRCh37 (hg19)		NC_000011.9	Chr11	99,647,049 (-1000, +500)	99,659,450 (-500, +1000)
essv22543253	Submitted genomic		NC_000011.9:g.(996 46049_99647549)_(9 9658950_99660450)d el	GRCh37 (hg19)		NC_000011.9	Chr11	99,647,049 (-1000, +500)	99,659,450 (-500, +1000)
essv22543254	Submitted genomic		NC_000011.9:g.(996 46049_99647549)_(9 9658950_99660450)d el	GRCh37 (hg19)		NC_000011.9	Chr11	99,647,049 (-1000, +500)	99,659,450 (-500, +1000)
essv22543255	Submitted genomic		NC_000011.9:g.(996 46049_99647549)_(9 9658950_99660450)d el	GRCh37 (hg19)		NC_000011.9	Chr11	99,647,049 (-1000, +500)	99,659,450 (-500, +1000)
essv22543256	Submitted genomic		NC_000011.9:g.(996 46049_99647549)_(9 9658950_99660450)d el	GRCh37 (hg19)		NC_000011.9	Chr11	99,647,049 (-1000, +500)	99,659,450 (-500, +1000)
essv22543257	Submitted genomic		NC_000011.9:g.(996 46049_99647549)_(9 9658950_99660450)d el	GRCh37 (hg19)		NC_000011.9	Chr11	99,647,049 (-1000, +500)	99,659,450 (-500, +1000)
essv22543258	Submitted genomic		NC_000011.9:g.(996 46049_99647549)_(9 9658950_99660450)d el	GRCh37 (hg19)		NC_000011.9	Chr11	99,647,049 (-1000, +500)	99,659,450 (-500, +1000)
essv22543259	Submitted genomic		NC_000011.9:g.(996 46049_99647549)_(9 9658950_99660450)d el	GRCh37 (hg19)		NC_000011.9	Chr11	99,647,049 (-1000, +500)	99,659,450 (-500, +1000)
essv22543260	Submitted genomic		NC_000011.9:g.(996 46049_99647549)_(9 9658950_99660450)d el	GRCh37 (hg19)		NC_000011.9	Chr11	99,647,049 (-1000, +500)	99,659,450 (-500, +1000)
essv22543261	Submitted genomic		NC_000011.9:g.(996 46049_99647549)_(9 9658950_99660450)d el	GRCh37 (hg19)		NC_000011.9	Chr11	99,647,049 (-1000, +500)	99,659,450 (-500, +1000)
essv22543262	Submitted genomic		NC_000011.9:g.(996 46049_99647549)_(9 9658950_99660450)d el	GRCh37 (hg19)		NC_000011.9	Chr11	99,647,049 (-1000, +500)	99,659,450 (-500, +1000)
essv22543263	Submitted genomic		NC_000011.9:g.(996 46049_99647549)_(9 9658950_99660450)d el	GRCh37 (hg19)		NC_000011.9	Chr11	99,647,049 (-1000, +500)	99,659,450 (-500, +1000)
essv22543264	Submitted genomic		NC_000011.9:g.(996 46049_99647549)_(9 9658950_99660450)d el	GRCh37 (hg19)		NC_000011.9	Chr11	99,647,049 (-1000, +500)	99,659,450 (-500, +1000)
essv22543265	Submitted genomic		NC_000011.9:g.(996 46049_99647549)_(9 9658950_99660450)d el	GRCh37 (hg19)		NC_000011.9	Chr11	99,647,049 (-1000, +500)	99,659,450 (-500, +1000)
essv22543266	Submitted genomic		NC_000011.9:g.(996 46049_99647549)_(9 9658950_99660450)d el	GRCh37 (hg19)		NC_000011.9	Chr11	99,647,049 (-1000, +500)	99,659,450 (-500, +1000)
essv22543267	Submitted genomic		NC_000011.9:g.(996 46049_99647549)_(9 9658950_99660450)d el	GRCh37 (hg19)		NC_000011.9	Chr11	99,647,049 (-1000, +500)	99,659,450 (-500, +1000)
essv22543268	Submitted genomic		NC_000011.9:g.(996 46049_99647549)_(9 9658950_99660450)d el	GRCh37 (hg19)		NC_000011.9	Chr11	99,647,049 (-1000, +500)	99,659,450 (-500, +1000)
essv22543269	Submitted genomic		NC_000011.9:g.(996 46049_99647549)_(9 9658950_99660450)d el	GRCh37 (hg19)		NC_000011.9	Chr11	99,647,049 (-1000, +500)	99,659,450 (-500, +1000)
essv22543270	Submitted genomic		NC_000011.9:g.(996 46049_99647549)_(9 9658950_99660450)d el	GRCh37 (hg19)		NC_000011.9	Chr11	99,647,049 (-1000, +500)	99,659,450 (-500, +1000)
essv22543271	Submitted genomic		NC_000011.9:g.(996 46049_99647549)_(9 9658950_99660450)d el	GRCh37 (hg19)		NC_000011.9	Chr11	99,647,049 (-1000, +500)	99,659,450 (-500, +1000)
essv22543272	Submitted genomic		NC_000011.9:g.(996 46049_99647549)_(9 9658950_99660450)d el	GRCh37 (hg19)		NC_000011.9	Chr11	99,647,049 (-1000, +500)	99,659,450 (-500, +1000)

dbVar

Database of genomic structural variation

esv3865261

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.