A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3448n100



Internal ID22789535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15666091..15683959hg38UCSC Ensembl
chr19:15776901..15794769hg19UCSC Ensembl
chr19:15637901..15655769hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3817869
hg1917869
hg1817869
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1063989, nsv1065694
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)dgv3448n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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