A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv452677



Internal ID18274584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32111694..32694378hg38UCSC Ensembl
Innerchr15:32403895..32986579hg19UCSC Ensembl
Innerchr15:30191187..30773871hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38582685
hg19582685
hg18582685
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428302
Supporting Variants
SamplesNA18916
Known GenesARHGAP11A, CHRNA7, GOLGA8K, GOLGA8O, GOLGA8R, LOC100996255, SCG5, ULK4P1, ULK4P2, ULK4P3, WHAMMP1
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)nssv452677
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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