A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893587



Internal ID18837721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:199189..204691hg38UCSC Ensembl
Outerchr3:199189..204691hg38UCSC Ensembl
Innerchr3:240872..246374hg19UCSC Ensembl
Outerchr3:240872..246374hg19UCSC Ensembl
Innerchr3:215872..221374hg18UCSC Ensembl
Outerchr3:215872..221374hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg385503
hg195503
hg185503
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25799021
Samples
Known GenesCHL1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893587
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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