A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1626n54



Internal ID20135050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:6735100..6877432hg38UCSC Ensembl
chr11:6756331..6898663hg19UCSC Ensembl
chr11:6712907..6855239hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38142333
hg19142333
hg18142333
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv553377, nsv553378, nsv553379
SamplesHGDP00807
Known GenesOR10A2, OR10A4, OR10A5, OR2AG1, OR2AG2, OR6A2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1626n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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