A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587390



Internal ID16028113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:33322014..33324196hg38UCSC Ensembl
Innerchr21:34694319..34696501hg19UCSC Ensembl
Innerchr21:33616189..33618371hg18UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg382183
hg192183
hg182183
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7817n54
Supporting Variantsnssv946638
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587390
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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