A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893804



Internal ID19184624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:163617018..164017426hg38UCSC Ensembl
Outerchr3:163617018..164017426hg38UCSC Ensembl
Innerchr3:163334806..163735214hg19UCSC Ensembl
Outerchr3:163334806..163735214hg19UCSC Ensembl
Innerchr3:164817500..165217908hg18UCSC Ensembl
Outerchr3:164817500..165217908hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38400409
hg19400409
hg18400409
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792300
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893804
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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