A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561853



Internal ID16349262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:58389683..58498005hg38UCSC Ensembl
Innerchr13:58963817..59072139hg19UCSC Ensembl
Innerchr13:57861818..57970140hg18UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg38108323
hg19108323
hg18108323
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv812324
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561853
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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