A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656726



Internal ID9922831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:95540542..95552092hg38UCSC Ensembl
Outerchr11:95540505..95552142hg38UCSC Ensembl
Innerchr11:95273706..95285256hg19UCSC Ensembl
Outerchr11:95273669..95285306hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3811638
hg1911638
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6218545
SamplesNA19717
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656726
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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