A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv452666



Internal ID18273673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31646275..32165340hg38UCSC Ensembl
Innerchr15:31938478..32457541hg19UCSC Ensembl
Innerchr15:29725770..30244833hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38519066
hg19519064
hg18519064
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428302
Supporting Variants
SamplesHGDP00474
Known GenesCHRNA7, OTUD7A
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)nssv452666
Frequency
Sample Size62
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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