A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv840246



Internal ID15787516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34438557..34546808hg38UCSC Ensembl
Innerchr15:34730758..34839009hg19UCSC Ensembl
Innerchr15:32518050..32626301hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38108252
hg19108252
hg18108252
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569066
Supporting Variants
Samples
Known GenesGOLGA8B, MIR1233-1, MIR1233-2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv840246
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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