A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv946614



Internal ID16240570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:33247140..33251614hg38UCSC Ensembl
Innerchr21:34619445..34623919hg19UCSC Ensembl
Innerchr21:33541315..33545789hg18UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg384475
hg194475
hg184475
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv587373
Supporting Variants
Samples
Known GenesIFNAR2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv946614
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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