A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587569



Internal ID16028292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:41870944..41890688hg38UCSC Ensembl
Innerchr21:43291053..43310797hg19UCSC Ensembl
Innerchr21:42164122..42183866hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3819745
hg1919745
hg1819745
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7851n54
Supporting Variantsnssv947148
Samples
Known GenesC2CD2, PRDM15
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587569
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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