A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14085949



Internal ID21290553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:102922046..102928125hg38UCSC Ensembl
Innerchr8:103934274..103940353hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg386080
hg196080
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111171
Supporting Variants
Samplessample60
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14085949
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