A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563158



Internal ID16350567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:110914229..110923567hg38UCSC Ensembl
Innerchr13:111566576..111575914hg19UCSC Ensembl
Innerchr13:110364577..110373915hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg389339
hg199339
hg189339
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv819913
Samples
Known GenesANKRD10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563158
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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