A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4566n100



Internal ID20156182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38729069..38782696hg38UCSC Ensembl
chr22:39125074..39178701hg19UCSC Ensembl
chr22:37455020..37508647hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3853628
hg1953628
hg1853628
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1062606, nsv1060365, nsv1059152, nsv1056287, nsv1066340
Samples
Known GenesDNAL4, GTPBP1, SUN2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4566n100
Frequency
Sample Size29084
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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