A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893622



Internal ID18837756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:2603842..2643965hg38UCSC Ensembl
Outerchr3:2603842..2664887hg38UCSC Ensembl
Innerchr3:2645526..2685649hg19UCSC Ensembl
Outerchr3:2645526..2706571hg19UCSC Ensembl
Innerchr3:2620526..2660649hg18UCSC Ensembl
Outerchr3:2620526..2681571hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3861046
hg1961046
hg1861046
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781723, essv25781782
Samples
Known GenesCNTN4
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893622
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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