A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1175991



Internal ID15854909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:70165521..70204085hg38UCSC Ensembl
Innerchr13:70739653..70778217hg19UCSC Ensembl
Innerchr13:69637654..69676218hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3838565
hg1938565
hg1838565
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv562240
Supporting Variants
Samples1780862384_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1175991
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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