A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv453868



Internal ID18274299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:64006869..64334167hg38UCSC Ensembl
Innerchr20:62638222..62965520hg19UCSC Ensembl
Innerchr20:62108666..62435964hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38327299
hg19327299
hg18327299
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428381
Supporting Variants
SamplesHGDP01093
Known GenesC20orf201, LINC00176, LINC00266-1, MIR6813, MYT1, NPBWR2, OPRL1, PCMTD2, PRPF6, RGS19, SOX18, TCEA2
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)nssv453868
Frequency
Sample Size62
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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