A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv453865



Internal ID18273227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:64006869..64274842hg38UCSC Ensembl
Innerchr20:62638222..62906195hg19UCSC Ensembl
Innerchr20:62108666..62376639hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38267974
hg19267974
hg18267974
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428381
Supporting Variants
SamplesHGDP00462
Known GenesC20orf201, LINC00176, 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)nssv453865
Frequency
Sample Size62
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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