A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3443n100



Internal ID22789530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15542560..15644632hg38UCSC Ensembl
chr19:15653371..15755442hg19UCSC Ensembl
chr19:15514371..15616442hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38102073
hg19102072
hg18102072
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1058037, nsv1061355, nsv1065872
Samples
Known GenesCYP4F22, CYP4F3, CYP4F8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3443n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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