A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1854n54



Internal ID22769749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:54525403..54756790hg38UCSC Ensembl
chr11:51362490..51593877hg19UCSC Ensembl
chr11:51219066..51450453hg18UCSC Ensembl
Cytoband11p11.11
Allele length
AssemblyAllele length
hg38231388
hg19231388
hg18231388
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv554591, nsv554588, nsv554589, nsv554587
Samples
Known GenesOR4A5, OR4C46
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1854n54
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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