A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14085864



Internal ID21285812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:89343653..89437794hg38UCSC Ensembl
Innerchr8:90355882..90450023hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3894142
hg1994142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112718
Supporting Variants
Samplessample38
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14085864
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