A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587659



Internal ID16028382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:42833569..42853748hg38UCSC Ensembl
Innerchr21:44253679..44273858hg19UCSC Ensembl
Innerchr21:43126748..43146927hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3820180
hg1920180
hg1820180
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv947403
Samples
Known GenesWDR4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587659
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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