A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25785895



Internal ID19174976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19812854..19932841hg38UCSC Ensembl
Innerchr14:20281013..20401000hg19UCSC Ensembl
Innerchr14:19350853..19470840hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38119988
hg19119988
hg18119988
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892457
Supporting Variants
Samples
Known GenesOR4K2, OR4K5, OR4N2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=7
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25785895
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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