A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569007



Internal ID16009730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34426604..34506266hg38UCSC Ensembl
Innerchr15:34718805..34798467hg19UCSC Ensembl
Innerchr15:32506097..32585759hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3879663
hg1979663
hg1879663
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4472n54
Supporting Variantsnssv840034
Samples
Known GenesGOLGA8A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569007
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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