A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568259



Internal ID16355668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22989526..23006570hg38UCSC Ensembl
Innerchr15:22866498..22883542hg19UCSC Ensembl
Innerchr15:20417939..20434983hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3817045
hg1917045
hg1817045
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv838385, nssv838384
Samples
Known GenesTUBGCP5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568259
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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