A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562140



Internal ID16349549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:67246371..67284418hg38UCSC Ensembl
Innerchr13:67820503..67858550hg19UCSC Ensembl
Innerchr13:66718504..66756551hg18UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg3838048
hg1938048
hg1838048
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv813413
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562140
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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