A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv452645



Internal ID18273567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:26275701..26641134hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg18365434
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428299
Supporting Variants
SamplesHGDP00472
Known GenesGOLGA8F, GOLGA8G, MIR4509-1, MIR4509-2, MIR4509-3
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)nssv452645
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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