A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv946616



Internal ID16240572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:33248146..33254349hg38UCSC Ensembl
Innerchr21:34620451..34626654hg19UCSC Ensembl
Innerchr21:33542321..33548524hg18UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg386204
hg196204
hg186204
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv587375
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)nssv946616
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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