A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613336



Internal ID16054059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:9801907..9816955hg38UCSC Ensembl
Innerchr9:9801907..9816955hg19UCSC Ensembl
Innerchr9:9791907..9806955hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3815049
hg1915049
hg1815049
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12509n54
Supporting Variantsnssv1126929
Samples
Known GenesPTPRD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613336
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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