A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562419



Internal ID16349828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:80102880..80112015hg38UCSC Ensembl
Innerchr13:80677015..80686150hg19UCSC Ensembl
Innerchr13:79575016..79584151hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg389136
hg199136
hg189136
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3271n54
Supporting Variantsnssv815916
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562419
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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