A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893608



Internal ID18837742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:1662983..2177012hg38UCSC Ensembl
Outerchr3:1662983..2177012hg38UCSC Ensembl
Innerchr3:1704667..2218696hg19UCSC Ensembl
Outerchr3:1704667..2218696hg19UCSC Ensembl
Innerchr3:1679667..2193696hg18UCSC Ensembl
Outerchr3:1679667..2193696hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38514030
hg19514030
hg18514030
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790333
Samples
Known GenesCNTN4, CNTN4-AS2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893608
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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