A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv819955



Internal ID16113911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:112015052..112015919hg38UCSC Ensembl
Innerchr13:112669366..112670233hg19UCSC Ensembl
Innerchr13:111717367..111718234hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38868
hg19868
hg18868
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv563190
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv819955
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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