A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066993



Internal ID19156212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15586172..15617341hg38UCSC Ensembl
Innerchr19:15696983..15728152hg19UCSC Ensembl
Innerchr19:15557983..15589152hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3831170
hg1931170
hg1831170
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564797
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)nsv1066993
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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