A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788368



Internal ID18824967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:124309052..124530715hg38UCSC Ensembl
Innerchr11:124178948..124400611hg19UCSC Ensembl
Innerchr11:123684158..123905821hg18UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38221664
hg19221664
hg18221664
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892105
Supporting Variants
Samples
Known GenesOR8B2, OR8B3, OR8B4, OR8B8, OR8D1, OR8D2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=42
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788368
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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