A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562089



Internal ID16349498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:65336660..65818859hg38UCSC Ensembl
Innerchr13:65910792..66392991hg19UCSC Ensembl
Innerchr13:64808793..65290992hg18UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg38482200
hg19482200
hg18482200
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3218n54
Supporting Variantsnssv1175941
Samples1780862162_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562089
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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