A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv450658



Internal ID18273480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32403976..32574849hg38UCSC Ensembl
Innerchr6:32371753..32542626hg19UCSC Ensembl
Innerchr6:32479731..32650604hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38170874
hg19170874
hg18170874
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428142
Supporting Variants
SamplesHGDP00471
Known GenesBTNL2, HLA-DRA, HLA-DRB5, HLA-DRB6
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)nssv450658
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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