A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv817861



Internal ID15765131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:98576676..98577650hg38UCSC Ensembl
Innerchr13:99228930..99229904hg19UCSC Ensembl
Innerchr13:98026931..98027905hg18UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg38975
hg19975
hg18975
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv562898
Supporting Variants
Samples
Known GenesSTK24
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv817861
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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