A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv454288



Internal ID18275097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162854370..163020518hg38UCSC Ensembl
Innerchr3:162572158..162738306hg19UCSC Ensembl
Innerchr3:164054852..164221000hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38166149
hg19166149
hg18166149
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428424
Supporting Variants
SamplesNA19181
Known Genes
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)nssv454288
Frequency
Sample Size62
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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