A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561860



Internal ID16349269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:59185421..59208414hg38UCSC Ensembl
Innerchr13:59759555..59782548hg19UCSC Ensembl
Innerchr13:58657556..58680549hg18UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg3822994
hg1922994
hg1822994
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv812334
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561860
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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