A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562417



Internal ID16349826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:79915679..80044780hg38UCSC Ensembl
Innerchr13:80489814..80618915hg19UCSC Ensembl
Innerchr13:79387815..79516916hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38129102
hg19129102
hg18129102
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv815914
Samples
Known GenesLINC01080
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562417
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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