A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv453099



Internal ID18274868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32222052..32692172hg38UCSC Ensembl
Innerchr16:32233373..32703493hg19UCSC Ensembl
Innerchr16:32140874..32610994hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38470121
hg19470121
hg18470121
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428325
Supporting Variants
SamplesNA19113
Known GenesLOC390705, TP53TG3, TP53TG3B, TP53TG3C, TP53TG3D
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)nssv453099
Frequency
Sample Size62
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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