A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893728



Internal ID19184548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:80605732..80988755hg38UCSC Ensembl
Outerchr3:80605732..80988755hg38UCSC Ensembl
Innerchr3:80654883..81037906hg19UCSC Ensembl
Outerchr3:80654883..81037906hg19UCSC Ensembl
Innerchr3:80737573..81120596hg18UCSC Ensembl
Outerchr3:80737573..81120596hg18UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg38383024
hg19383024
hg18383024
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788030
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893728
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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