A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788851



Internal ID19176842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:143882155..144016702hg38UCSC Ensembl
Innerchr3:143600997..143735544hg19UCSC Ensembl
Innerchr3:145083687..145218234hg18UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38134548
hg19134548
hg18134548
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893777
Supporting Variants
Samples
Known GenesC3orf58
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=20
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788851
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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