A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663388



Internal ID9929493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:61100013..61100136hg38UCSC Ensembl
Outerchr11:61099976..61100186hg38UCSC Ensembl
Innerchr11:60867485..60867608hg19UCSC Ensembl
Outerchr11:60867448..60867658hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38211
hg19211
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5785976, essv6142701, essv5790083, essv5992236, essv5639207, essv5519304, essv5488961, essv6330335, essv6563514, essv5899613, essv5734396, essv6283048, essv6019445, essv6190399, essv5406699, essv5964548, essv6526381, essv5680529, essv6492855, essv5991733, essv6526749, essv5651817, essv6287342, essv6439908, essv6183637, essv5625649, essv5419506, essv6477123, essv5879914, essv6292683, essv5799481, essv5716672, essv6287072, essv6190645, essv5788489
SamplesHG00524, HG01188, HG00257, HG00315, HG00699, NA18530, HG00449, HG01051, HG00693, NA18964, HG00537, HG00512, HG00277, HG01080, HG00335, HG01072, HG00534, HG00338, HG00419, NA19391, NA19663, HG00533, HG00500, HG00619, HG01047, HG00690, NA18532, HG00140, NA19732, HG00421, HG00656, HG00342, HG00698, NA18622, HG01061
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663388
Frequency
Sample Size1151
Observed Gain0
Observed Loss35
Observed Complex0
Frequencyn/a


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