A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv839808



Internal ID15787078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34392403..34552372hg38UCSC Ensembl
Innerchr15:34684604..34844573hg19UCSC Ensembl
Innerchr15:32471896..32631865hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38159970
hg19159970
hg18159970
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv568932
Supporting Variants
Samples
Known GenesGOLGA8A, GOLGA8B, MIR1233-1, MIR1233-2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv839808
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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