A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25791452



Internal ID18821701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105686797..106289177hg38UCSC Ensembl
Innerchr14:106153134..106745771hg19UCSC Ensembl
Innerchr14:105224179..105816816hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38602381
hg19592638
hg18592638
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892584
Supporting Variants
Samples
Known GenesADAM6, KIAA0125, LINC00226
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=36
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25791452
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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