A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892457



Internal ID19183277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19837272..19932841hg38UCSC Ensembl
Outerchr14:19797042..19989329hg38UCSC Ensembl
Innerchr14:20305431..20401000hg19UCSC Ensembl
Outerchr14:20265201..20457488hg19UCSC Ensembl
Innerchr14:19375271..19470840hg18UCSC Ensembl
Outerchr14:19335041..19527328hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38192288
hg19192288
hg18192288
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792831, essv25789367, essv25792366, essv25790217, essv25789038, essv25789438, essv25792677, essv25800621, essv25788570, essv25792964, essv25789440, essv25799835, essv25785895, essv25788770
Samples
Known GenesOR4K1, OR4K15, OR4K2, OR4K5, OR4N2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892457
Frequency
Sample Size3017
Observed Gain11
Observed Loss3
Observed Complex0
Frequencyn/a


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