A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788712



Internal ID18832205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55315958..55698436hg38UCSC Ensembl
Innerchr11:55083434..55465912hg19UCSC Ensembl
Innerchr11:54840010..55222488hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38382479
hg19382479
hg18382479
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892009
Supporting Variants
Samples
Known GenesOR4A15, OR4A16, OR4C11, OR4C15, OR4C16, OR4C6, OR4P4, OR4S2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=84
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788712
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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