A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv56n21



Internal ID20131777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5352021..5352332hg38UCSC Ensembl
chr11:5373251..5373562hg19UCSC Ensembl
chr11:5329827..5330138hg18UCSC Ensembl
chr11:5329827..5330138hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38312
hg19312
hg18312
hg17312
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv521732, nsv525848
Samples
Known GenesOR51B5, OR51B6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv56n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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