A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562935



Internal ID16350344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:99086152..99110367hg38UCSC Ensembl
Innerchr13:99738406..99762621hg19UCSC Ensembl
Innerchr13:98536407..98560622hg18UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg3824216
hg1924216
hg1824216
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv818096
Samples
Known GenesDOCK9, DOCK9-AS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562935
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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