A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613342



Internal ID16054065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:9803954..9855408hg38UCSC Ensembl
Innerchr9:9803954..9855408hg19UCSC Ensembl
Innerchr9:9793954..9845408hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3851455
hg1951455
hg1851455
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12506n54
Supporting Variantsnssv1126935
Samples
Known GenesPTPRD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613342
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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