A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562942



Internal ID16350351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:99086622..99087408hg38UCSC Ensembl
Innerchr13:99738876..99739662hg19UCSC Ensembl
Innerchr13:98536877..98537663hg18UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg38787
hg19787
hg18787
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv818109
Samples
Known GenesDOCK9-AS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562942
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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