A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv820113



Internal ID16114069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:112195741..112215343hg38UCSC Ensembl
Innerchr13:112850055..112869657hg19UCSC Ensembl
Innerchr13:111898056..111917658hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3819603
hg1919603
hg1819603
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv563204
Supporting Variants
Samples
Known GenesLINC01070
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv820113
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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