A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv812337



Internal ID15759607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:60419209..60537663hg38UCSC Ensembl
Innerchr13:60993343..61111797hg19UCSC Ensembl
Innerchr13:59891344..60009798hg18UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg38118455
hg19118455
hg18118455
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv561864
Supporting Variants
Samples
Known GenesTDRD3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv812337
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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