A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792366



Internal ID19164649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19797042..19948340hg38UCSC Ensembl
Innerchr14:20265201..20416499hg19UCSC Ensembl
Innerchr14:19335041..19486339hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38151299
hg19151299
hg18151299
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892457
Supporting Variants
Samples
Known GenesOR4K1, OR4K2, OR4K5, OR4N2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=12
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792366
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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