A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3453n100



Internal ID22789540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15688466..15714929hg38UCSC Ensembl
chr19:15799276..15825739hg19UCSC Ensembl
chr19:15660276..15686739hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3826464
hg1926464
hg1826464
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1065116, nsv1062293
Samples
Known GenesCYP4F12
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3453n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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