A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613322



Internal ID16054045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:9790222..9805134hg38UCSC Ensembl
Innerchr9:9790222..9805134hg19UCSC Ensembl
Innerchr9:9780222..9795134hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3814913
hg1914913
hg1814913
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1126913
Samples
Known GenesPTPRD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613322
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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