A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25784502



Internal ID18829868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55614418..55685447hg38UCSC Ensembl
Innerchr11:55381894..55452923hg19UCSC Ensembl
Innerchr11:55138470..55209499hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3871030
hg1971030
hg1871030
Variant TypeCNV loss
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892006
Supporting Variants
Samples
Known GenesOR4C6, OR4P4, OR4S2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=30
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25784502
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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