A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893683



Internal ID19184503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:37938391..37951049hg38UCSC Ensembl
Outerchr3:37938391..37951049hg38UCSC Ensembl
Innerchr3:37979882..37992540hg19UCSC Ensembl
Outerchr3:37979882..37992540hg19UCSC Ensembl
Innerchr3:37954886..37967544hg18UCSC Ensembl
Outerchr3:37954886..37967544hg18UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3812659
hg1912659
hg1812659
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25798167
Samples
Known GenesCTDSPL
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893683
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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