A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561482



Internal ID16348891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:35070815..35100896hg38UCSC Ensembl
Innerchr13:35644952..35675033hg19UCSC Ensembl
Innerchr13:34542952..34573033hg18UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg3830082
hg1930082
hg1830082
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv807721
Samples
Known GenesNBEA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561482
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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