A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14108076



Internal ID21282838
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 StatusS
Merged Variantsnsv3115479
Supporting Variants
Samplessample332
Known GenesFGF12
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14108076
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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