A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626459



Internal ID7013291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:55893951..55967305hg38UCSC Ensembl
chr11:55661427..55734781hg19UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3873355
hg1973355
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14165605, essv14165601, essv14165600, essv14165593, essv14165597, essv14165592, essv14165596, essv14165604, essv14165603, essv14165598, essv14165595, essv14165599, essv14165594, essv14165606, essv14165602
SamplesHG03163, HG03111, HG03130, HG03193, HG03133, HG03189, HG03114, HG02977, HG03311, HG03136, HG00565, NA18876, NA19213, NA18488, HG03166
Known GenesOR5I1, OR5W2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626459
Frequency
Sample Size2504
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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