A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv428356



Internal ID18624806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:67274550..67423722hg38UCSC Ensembl
Innerchr18:64941787..65090959hg19UCSC Ensembl
Innerchr18:63092767..63241939hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38149173
hg19149173
hg18149173
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv453591
SamplesNA18916
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)nsv428356
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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