A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568928



Internal ID16009651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34380544..34490724hg38UCSC Ensembl
Innerchr15:34672745..34782925hg19UCSC Ensembl
Innerchr15:32460037..32570217hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38110181
hg19110181
hg18110181
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4458n54
Supporting Variantsnssv839804
Samples
Known GenesGOLGA8A, MIR1233-1, MIR1233-2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568928
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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