A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4477n54



Internal ID18996653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34426604..34604990hg38UCSC Ensembl
chr15:34718805..34897191hg19UCSC Ensembl
chr15:32506097..32684483hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38178387
hg19178387
hg18178387
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv569010, nsv569068
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)dgv4477n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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