A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14105164



Internal ID21278083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:76531070..76546294hg38UCSC Ensembl
Innerchr2:76758196..76773420hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3815225
hg1915225
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112169
Supporting Variants
Samplessample263
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14105164
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer