A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563160



Internal ID16350569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:110914462..110915799hg38UCSC Ensembl
Innerchr13:111566809..111568146hg19UCSC Ensembl
Innerchr13:110364810..110366147hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381338
hg191338
hg181338
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv819916, nssv819915, nssv819917
Samples
Known GenesANKRD10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563160
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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