A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv454224



Internal ID18621595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:20334758..20499136hg38UCSC Ensembl
Innerchr3:20376250..20540628hg19UCSC Ensembl
Innerchr3:20351254..20515632hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38164379
hg19164379
hg18164379
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428414
Supporting Variants
SamplesNA19113
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)nssv454224
Frequency
Sample Size62
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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