A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562090



Internal ID16349499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:65357221..65934212hg38UCSC Ensembl
Innerchr13:65931353..66508344hg19UCSC Ensembl
Innerchr13:64829354..65406345hg18UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg38576992
hg19576992
hg18576992
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3218n54
Supporting Variantsnssv1175942
SamplesHGDP00224
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562090
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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