A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563232



Internal ID16350641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:112762663..112767444hg38UCSC Ensembl
Innerchr13:113416977..113421758hg19UCSC Ensembl
Innerchr13:112464978..112469759hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg384782
hg194782
hg184782
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv820158
Samples
Known GenesATP11A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563232
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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