A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv454382



Internal ID18274732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:8591986..9123666hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg18531681
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428437
Supporting Variants
SamplesNA19108
Known GenesCPZ, DEFB131, GPR78, LOC650293, USP17L10, USP17L11, USP17L12, USP17L13, USP17L15, USP17L17, USP17L18, USP17L19, USP17L20, USP17L21, USP17L22, USP17L24, USP17L25, USP17L26, USP17L27, USP17L28, USP17L29, USP17L30, USP17L5, USP17L6P, USP17L9P
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)nssv454382
Frequency
Sample Size62
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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