A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626992



Internal ID7013822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:82213435..82338021hg38UCSC Ensembl
Innerchr11:82213479..82337977hg38UCSC Ensembl
Outerchr11:82213391..82338065hg38UCSC Ensembl
chr11:81924477..82049063hg19UCSC Ensembl
Innerchr11:81924521..82049019hg19UCSC Ensembl
Outerchr11:81924433..82049107hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38124587
hg19124587
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv213e214
Supporting Variantsessv14218755
SamplesNA20771
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626992
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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