A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587387



Internal ID16028110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:33321963..33326080hg38UCSC Ensembl
Innerchr21:34694268..34698385hg19UCSC Ensembl
Innerchr21:33616138..33620255hg18UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg384118
hg194118
hg184118
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv946635
Samples
Known GenesIFNAR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587387
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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