A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv428425



Internal ID18624875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:163884661..164192272hg38UCSC Ensembl
Innerchr3:163602449..163910060hg19UCSC Ensembl
Innerchr3:165085143..165392754hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38307612
hg19307612
hg18307612
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv454290
SamplesHGDP00462
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)nsv428425
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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