A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111536



Internal ID21294802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:115959724..115979929hg38UCSC Ensembl
Innerchr8:116971949..116992154hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3820206
hg1920206
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14087484
Samplessample345
Known GenesLINC00536
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111536
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