A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25789654



Internal ID19174892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55836936..55922895hg38UCSC Ensembl
Innerchr11:55604412..55690371hg19UCSC Ensembl
Innerchr11:55360988..55446947hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3885960
hg1985960
hg1885960
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892013
Supporting Variants
Samples
Known GenesOR5D16, OR5W2, TRIM51
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=40
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25789654
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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