A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115479



Internal ID21298745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:192220115..192269654hg38UCSC Ensembl
Innerchr3:191937904..191987443hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3849540
hg1949540
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv839n145
Supporting Variantsnssv14108505, nssv14108076
Samplessample346, sample332
Known GenesFGF12
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115479
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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