A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14109392



Internal ID21282566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:17316157..17319517hg38UCSC Ensembl
Innerchr5:17316266..17319626hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg383361
hg193361
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112274
Supporting Variants
Samplessample329
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14109392
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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