A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3447n100



Internal ID22789534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15661423..15723148hg38UCSC Ensembl
chr19:15772233..15833958hg19UCSC Ensembl
chr19:15633233..15694958hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3861726
hg1961726
hg1861726
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1060322, nsv1064359, nsv1062490, nsv1064145, nsv1058512, nsv1058473, nsv1066177, nsv1056906, nsv1061283, nsv1063072, nsv1056457, nsv1065077
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)dgv3447n100
Frequency
Sample Size11257
Observed Gain33
Observed Loss0
Observed Complex0
Frequencyn/a


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