A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv839n145



Internal ID22813855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:192220115..192269654hg38UCSC Ensembl
chr3:191937904..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 Variants
Supporting Variantsnsv3115479, nsv3114187
Samplessample346, sample312, sample332
Known GenesFGF12
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv839n145
Frequency
Sample Size467
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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