A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893777



Internal ID19184597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:143882155..144016702hg38UCSC Ensembl
Outerchr3:143882155..144016702hg38UCSC Ensembl
Innerchr3:143600997..143735544hg19UCSC Ensembl
Outerchr3:143600997..143735544hg19UCSC Ensembl
Innerchr3:145083687..145218234hg18UCSC Ensembl
Outerchr3:145083687..145218234hg18UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38134548
hg19134548
hg18134548
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788851
Samples
Known GenesC3orf58
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893777
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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