A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587368



Internal ID16028091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:33228716..33231233hg38UCSC Ensembl
Innerchr21:34601021..34603538hg19UCSC Ensembl
Innerchr21:33522891..33525408hg18UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg382518
hg192518
hg182518
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv946609
Samples
Known GenesIFNAR2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587368
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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