A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4458n54



Internal ID18996634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34379904..34490724hg38UCSC Ensembl
chr15:34672105..34782925hg19UCSC Ensembl
chr15:32459397..32570217hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38110821
hg19110821
hg18110821
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv568927, nsv568930, nsv568928
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)dgv4458n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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