A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562874



Internal ID16003597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:98575484..98576728hg38UCSC Ensembl
Innerchr13:99227738..99228982hg19UCSC Ensembl
Innerchr13:98025739..98026983hg18UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg381245
hg191245
hg181245
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv817782
Samples
Known GenesSTK24
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562874
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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