A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1941n54



Internal ID22769836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:55679951..55836936hg38UCSC Ensembl
chr11:55447427..55604412hg19UCSC Ensembl
chr11:55204003..55360988hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38156986
hg19156986
hg18156986
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv555075, nsv555060, nsv555061
SamplesHGDP00926, HGDP00940
Known GenesOR5D13, OR5D14, OR5D18, OR5L1, OR5L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1941n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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