A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv453167



Internal ID18273288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:33067153..33571953hg38UCSC Ensembl
Innerchr16:33078474..33374420hg19UCSC Ensembl
Innerchr16:32985975..33281921hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38504801
hg19295947
hg18295947
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428325
Supporting Variants
SamplesHGDP00462
Known GenesLOC390705, TP53TG3, 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)nssv453167
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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