A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv453094



Internal ID18272955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32222052..32286366hg38UCSC Ensembl
Innerchr16:32233373..32297687hg19UCSC Ensembl
Innerchr16:32140874..32205188hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3864315
hg1964315
hg1864315
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428325
Supporting Variants
SamplesHGDP00449
Known GenesTP53TG3D
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)nssv453094
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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