A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4013459



Internal ID22075090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15879621..15893672hg38UCSC Ensembl
Outerchr19:15873932..15901947hg38UCSC Ensembl
Innerchr19:15990431..16004482hg19UCSC Ensembl
Outerchr19:15984742..16012757hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3828016
hg1928016
Variant TypeCNV duplication
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155558
Supporting Variants
Samples
Known GenesCYP4F2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4013459
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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