A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14109018



Internal ID21275145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:27158039..27234134hg38UCSC Ensembl
Innerchr5:27158146..27234241hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3876096
hg1976096
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115679
Supporting Variants
Samplessample217
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14109018
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