A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv456n21



Internal ID20132177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:28321496..28467894hg38UCSC Ensembl
chr8:28179013..28325411hg19UCSC Ensembl
chr8:28234932..28381330hg18UCSC Ensembl
chr8:28234932..28381330hg17UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg38146399
hg19146399
hg18146399
hg17146399
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv518985, nsv524153
Samples
Known GenesFBXO16, PNOC, ZNF395
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv456n21
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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