A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113014



Internal ID21296280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:116156261..116162278hg38UCSC Ensembl
Innerchr8:117168486..117174503hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg386018
hg196018
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14088185
Samplessample372
Known GenesLINC00536
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113014
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