A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587394



Internal ID16028117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:33323618..33325209hg38UCSC Ensembl
Innerchr21:34695923..34697514hg19UCSC Ensembl
Innerchr21:33617793..33619384hg18UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg381592
hg191592
hg181592
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv946644
Samples
Known GenesIFNAR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587394
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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