A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626453



Internal ID7013285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:55691646..55841751hg38UCSC Ensembl
chr11:55459122..55609227hg19UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38150106
hg19150106
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14165459, essv14165457, essv14165454, essv14165463, essv14165462, essv14165465, essv14165470, essv14165472, essv14165467, essv14165469, essv14165455, essv14165474, essv14165453, essv14165458, essv14165464, essv14165473, essv14165461, essv14165466, essv14165471, essv14165468, essv14165460, essv14165456
SamplesHG02614, HG03449, HG02471, HG02588, NA19239, NA19209, HG03394, HG03169, HG02943, HG02439, HG00731, NA19437, NA19347, HG01889, NA19225, NA19435, HG01375, NA19376, HG02974, NA19351, NA19093, HG03265
Known GenesOR5D13, OR5D14, OR5D16, OR5D18, OR5L1, OR5L2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626453
Frequency
Sample Size2504
Observed Gain0
Observed Loss22
Observed Complex0
Frequencyn/a


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