A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790764



Internal ID19160333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19717840..19969990hg38UCSC Ensembl
Innerchr14:20185999..20438149hg19UCSC Ensembl
Innerchr14:19255839..19507989hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38252151
hg19252151
hg18252151
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892451
Supporting Variants
Samples
Known GenesOR4K1, OR4K2, OR4K5, OR4M1, OR4N2, OR4Q3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=26
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790764
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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