A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562364



Internal ID16349773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:76482780..76644438hg38UCSC Ensembl
Innerchr13:77056916..77218573hg19UCSC Ensembl
Innerchr13:75954917..76116574hg18UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg38161659
hg19161658
hg18161658
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv815786
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562364
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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