A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788374



Internal ID19176278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19717840..19948340hg38UCSC Ensembl
Innerchr14:20185999..20416499hg19UCSC Ensembl
Innerchr14:19255839..19486339hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38230501
hg19230501
hg18230501
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=22
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788374
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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