A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115183



Internal ID21298449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:80084488..80110048hg38UCSC Ensembl
Innerchr2:80311614..80337174hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3825561
hg1925561
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14106073
Samplessample299
Known GenesCTNNA2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115183
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