A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4802n54



Internal ID20138226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:101788321..101858428hg38UCSC Ensembl
chr15:102328524..102398631hg19UCSC Ensembl
chr15:100146047..100216154hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3870108
hg1970108
hg1870108
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv570914, nsv570913
Samples
Known GenesOR4F13P, OR4F15, OR4F6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4802n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer