A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790333



Internal ID18829736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:1662983..2177012hg38UCSC Ensembl
Innerchr3:1704667..2218696hg19UCSC Ensembl
Innerchr3:1679667..2193696hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38514030
hg19514030
hg18514030
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893608
Supporting Variants
Samples
Known GenesCNTN4, CNTN4-AS2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=209
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790333
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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