A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14094709



Internal ID21284427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:161272388..161281375hg38UCSC Ensembl
Innerchr4:162193540..162202527hg19UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg388988
hg198988
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112119
Supporting Variants
Samplessample360
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14094709
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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