A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562145



Internal ID16349554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:68230616..68326220hg38UCSC Ensembl
Innerchr13:68804748..68900352hg19UCSC Ensembl
Innerchr13:67702749..67798353hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3895605
hg1995605
hg1895605
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv813416
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562145
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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