A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057215



Internal ID19146434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15617292..15648121hg38UCSC Ensembl
Innerchr19:15728103..15758931hg19UCSC Ensembl
Innerchr19:15589103..15619931hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3830830
hg1930829
hg1830829
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3445n100
Supporting Variantsnssv3564804
Samples
Known GenesCYP4F3, CYP4F8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057215
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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