A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3445n100



Internal ID22789532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15613287..15648121hg38UCSC Ensembl
chr19:15724098..15758931hg19UCSC Ensembl
chr19:15585098..15619931hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3834835
hg1934834
hg1834834
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1055298, nsv1057215, nsv1063515
Samples
Known GenesCYP4F3, CYP4F8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3445n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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