A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587367



Internal ID16028090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:33222573..33230523hg38UCSC Ensembl
Innerchr21:34594878..34602828hg19UCSC Ensembl
Innerchr21:33516748..33524698hg18UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg387951
hg197951
hg187951
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv946608
Samples
Known GenesIFNAR2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587367
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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