A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv428415



Internal ID18624865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:22036401..22215377hg38UCSC Ensembl
Innerchr3:22077893..22256869hg19UCSC Ensembl
Innerchr3:22052897..22231873hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38178977
hg19178977
hg18178977
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv454231
SamplesHGDP00476
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)nsv428415
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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