A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv428424



Internal ID18278188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162428200..163316155hg38UCSC Ensembl
Innerchr3:162145988..163033943hg19UCSC Ensembl
Innerchr3:163628682..164516637hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38887956
hg19887956
hg18887956
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv454284, nssv454286, nssv454288, nssv454285
SamplesHGDP01088, NA18916, NA19181, HGDP00449
Known GenesCT64
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)nsv428424
Frequency
Sample Size62
Observed Gain3
Observed Loss1
Observed Complex0
Frequencyn/a


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