A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14108774



Internal ID21270972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:57725153..57769807hg38UCSC Ensembl
Innerchr5:57020980..57065634hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3844655
hg1944655
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114413
Supporting Variants
Samplessample157
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14108774
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