A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4495n54



Internal ID22772390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:38891229..39098052hg38UCSC Ensembl
chr15:39183430..39390253hg19UCSC Ensembl
chr15:36970722..37177545hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38206824
hg19206824
hg18206824
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv569210, nsv569207, nsv569209, nsv569211, nsv569208
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4495n54
Frequency
Sample Size17421
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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