A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14096748



Internal ID21278463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:98072851..98312510hg38UCSC Ensembl
Innerchr5:97408555..97648214hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38239660
hg19239660
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116715
Supporting Variants
Samplessample27
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14096748
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