A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893846



Internal ID19184666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:191988170..192090302hg38UCSC Ensembl
Outerchr3:191988170..192090302hg38UCSC Ensembl
Innerchr3:191705959..191808091hg19UCSC Ensembl
Outerchr3:191705959..191808091hg19UCSC Ensembl
Innerchr3:193188653..193290785hg18UCSC Ensembl
Outerchr3:193188653..193290785hg18UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg38102133
hg19102133
hg18102133
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792112
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893846
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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