A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613037



Internal ID16053760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:643453..1138368hg38UCSC Ensembl
Innerchr9:643453..1138368hg19UCSC Ensembl
Innerchr9:633453..1128368hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38494916
hg19494916
hg18494916
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1125996
Samples
Known GenesDMRT1, DMRT2, DMRT3, KANK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613037
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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