A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25791375



Internal ID19172000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19616004..19941099hg38UCSC Ensembl
Innerchr14:20084006..20409258hg19UCSC Ensembl
Innerchr14:19154003..19479098hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38325096
hg19325253
hg18325096
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892464
Supporting Variants
Samples
Known GenesOR11H2, OR4K1, OR4K2, OR4K5, OR4M1, OR4N2, OR4Q3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=56
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25791375
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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