A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893733



Internal ID19184553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:84016952..84057090hg38UCSC Ensembl
Outerchr3:84016952..84057090hg38UCSC Ensembl
Innerchr3:84066103..84106241hg19UCSC Ensembl
Outerchr3:84066103..84106241hg19UCSC Ensembl
Innerchr3:84148793..84188931hg18UCSC Ensembl
Outerchr3:84148793..84188931hg18UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3840139
hg1940139
hg1840139
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25801315, essv25801298, essv25797534
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893733
Frequency
Sample Size3017
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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