A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790901



Internal ID19170174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19711892..19932841hg38UCSC Ensembl
Innerchr14:20180051..20401000hg19UCSC Ensembl
Innerchr14:19249891..19470840hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38220950
hg19220950
hg18220950
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892451
Supporting Variants
Samples
Known GenesOR11H2, OR4K2, OR4K5, OR4M1, OR4N2, OR4Q3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=20
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790901
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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