A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3567503



Internal ID18865784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40991369..41052366hg38UCSC Ensembl
Innerchr19:41497274..41558271hg19UCSC Ensembl
Innerchr19:46189114..46250111hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3860998
hg1960998
hg1860998
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058051
Supporting Variants
Samples
Known GenesCYP2B6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3567503
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