A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561680



Internal ID16349089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:53660504..53666096hg38UCSC Ensembl
Innerchr13:54234639..54240231hg19UCSC Ensembl
Innerchr13:53132640..53138232hg18UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg385593
hg195593
hg185593
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv811723
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561680
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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