A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613335



Internal ID16054058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:9800624..9855408hg38UCSC Ensembl
Innerchr9:9800624..9855408hg19UCSC Ensembl
Innerchr9:9790624..9845408hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3854785
hg1954785
hg1854785
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1126928
Samples
Known GenesPTPRD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613335
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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