A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv453111



Internal ID18273961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32428787..32692172hg38UCSC Ensembl
Innerchr16:32440108..32703493hg19UCSC Ensembl
Innerchr16:32347609..32610994hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38263386
hg19263386
hg18263386
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428325
Supporting Variants
SamplesHGDP00986
Known GenesTP53TG3, TP53TG3B, TP53TG3C
MethodBAC aCGH
AnalysisCopy number variable segments were automatically detected using the CNVfinder algorithm (Fiegler et al. 2006).
PlatformSanger H. sapiens Whole Genome Tile Path 28.7k v3
Comments
ReferencePerry_et_al_2008b
Pubmed ID18775914
Accession Number(s)nssv453111
Frequency
Sample Size62
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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