A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562875



Internal ID16003598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:98575484..98577597hg38UCSC Ensembl
Innerchr13:99227738..99229851hg19UCSC Ensembl
Innerchr13:98025739..98027852hg18UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg382114
hg192114
hg182114
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv817783, nssv817784
Samples
Known GenesSTK24
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562875
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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