A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561649



Internal ID16002372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:51917057..51996592hg38UCSC Ensembl
Innerchr13:52491193..52570728hg19UCSC Ensembl
Innerchr13:51389194..51468729hg18UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg3879536
hg1979536
hg1879536
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv811674
Samples
Known GenesATP7B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561649
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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