A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5009n100



Internal ID22791096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:192214698..192230051hg38UCSC Ensembl
chr3:191932487..191947840hg19UCSC Ensembl
chr3:193415181..193430534hg18UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3815354
hg1915354
hg1815354
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1006637, nsv998673, nsv1002460
Samples
Known GenesFGF12
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5009n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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