A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065986



Internal ID18808517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15667121..15714929hg38UCSC Ensembl
Innerchr19:15777931..15825739hg19UCSC Ensembl
Innerchr19:15638931..15686739hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3847809
hg1947809
hg1847809
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3446n100
Supporting Variantsnssv3564825, nssv3564823, nssv3564824, nssv3564826, nssv3564827
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)nsv1065986
Frequency
Sample Size29084
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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