A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561353



Internal ID16348762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:25464171..25510023hg38UCSC Ensembl
Innerchr13:26038309..26084161hg19UCSC Ensembl
Innerchr13:24936309..24982161hg18UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg3845853
hg1945853
hg1845853
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv806779
Samples
Known GenesATP8A2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561353
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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