A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4475n54



Internal ID18996651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34426393..34740655hg38UCSC Ensembl
chr15:34718594..35032856hg19UCSC Ensembl
chr15:32505886..32820148hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38314263
hg19314263
hg18314263
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv569129, nsv569005
Samples
Known GenesGOLGA8A, GOLGA8B, MIR1233-1, MIR1233-2, MIR5588
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4475n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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