A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587372



Internal ID16374781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:33246008..33249643hg38UCSC Ensembl
Innerchr21:34618313..34621948hg19UCSC Ensembl
Innerchr21:33540183..33543818hg18UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg383636
hg193636
hg183636
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv946613
Samples
Known GenesIFNAR2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587372
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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