A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv40e55



Internal ID22760990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5864481..5947955hg38UCSC Ensembl
chr11:5885711..5969185hg19UCSC Ensembl
chr11:5842287..5925761hg18UCSC Ensembl
chr11:5842287..5925761hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3883475
hg1983475
hg1883475
hg1783475
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv34821, esv34778
SamplesNA18571, NA18994
Known GenesOR52E4, OR56A3
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)dgv40e55
Frequency
Sample Size771
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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