A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv453433



Internal ID18274571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:33376129..33649123hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg18272995
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428341
Supporting Variants
SamplesNA18916
Known GenesLOC440434, TBC1D3, TBC1D3C, TBC1D3F
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)nssv453433
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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