A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3564941



Internal ID18863222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15669231..15723148hg38UCSC Ensembl
Innerchr19:15780041..15833958hg19UCSC Ensembl
Innerchr19:15641041..15694958hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3853918
hg1953918
hg1853918
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1063072
Supporting Variants
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)nssv3564941
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