A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626458



Internal ID7013290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:55838330..55932729hg38UCSC Ensembl
chr11:55605806..55700205hg19UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3894400
hg1994400
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14165588, essv14165590, essv14165591, essv14165589
SamplesHG00881, HG00346, HG03563, HG00371
Known GenesOR5D16, OR5W2, TRIM51
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626458
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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