A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114816



Internal ID21298082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:74451771..74454989hg38UCSC Ensembl
Innerchr8:75364006..75367224hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg383219
hg193219
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14087335
Samplessample305
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114816
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