A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892009



Internal ID18839719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55315958..55592737hg38UCSC Ensembl
Outerchr11:55167087..55698436hg38UCSC Ensembl
Innerchr11:55083434..55360213hg19UCSC Ensembl
Outerchr11:54934563..55465912hg19UCSC Ensembl
Innerchr11:54840010..55116789hg18UCSC Ensembl
Outerchr11:54691139..55222488hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38531350
hg19531350
hg18531350
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790227, essv25788712
Samples
Known GenesOR4A15, OR4A16, OR4C11, OR4C15, OR4C16, OR4C6, OR4P4, OR4S2, TRIM48, TRIM51HP
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892009
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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