A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3444n100



Internal ID22789531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15609874..15638182hg38UCSC Ensembl
chr19:15720685..15748992hg19UCSC Ensembl
chr19:15581685..15609992hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3828309
hg1928308
hg1828308
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1059028, nsv1065592
Samples
Known GenesCYP4F8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3444n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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