A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3446n100



Internal ID20155062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15661423..15714929hg38UCSC Ensembl
chr19:15772233..15825739hg19UCSC Ensembl
chr19:15633233..15686739hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3853507
hg1953507
hg1853507
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1061767, nsv1066845, nsv1059204, nsv1066010, nsv1063569, nsv1057838, nsv1056601, nsv1063313, nsv1066905, nsv1057813, nsv1062259, nsv1060333, nsv1065577, nsv1065166, nsv1058441, nsv1057961, nsv1067246, nsv1062649, nsv1059348, nsv1065977, nsv1065986, nsv1063891, nsv1057902, nsv1059151, nsv1061202, nsv1055441, nsv1065885, nsv1063051
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)dgv3446n100
Frequency
Sample Size29084
Observed Gain153
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer