A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv946617



Internal ID15893887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:33271777..33307426hg38UCSC Ensembl
Innerchr21:34644082..34679731hg19UCSC Ensembl
Innerchr21:33565952..33601601hg18UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3835650
hg1935650
hg1835650
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv587376
Supporting Variants
Samples
Known GenesIL10RB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv946617
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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