A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562890



Internal ID16003613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:98576401..98577256hg38UCSC Ensembl
Innerchr13:99228655..99229510hg19UCSC Ensembl
Innerchr13:98026656..98027511hg18UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg38856
hg19856
hg18856
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv817844, nssv817845
Samples
Known GenesSTK24
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562890
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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