A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14108398



Internal ID21269250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:64429075..64499568hg38UCSC Ensembl
Innerchr5:63724902..63795395hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg3870494
hg1970494
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110358
Supporting Variants
Samplessample137
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14108398
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