A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv450843



Internal ID18621802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:103279946..103357128hg38UCSC Ensembl
Innerchr6:103727821..103805003hg19UCSC Ensembl
Innerchr6:103834514..103911696hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3877183
hg1977183
hg1877183
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428152
Supporting Variants
SamplesNA19189
Known Genes
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)nssv450843
Frequency
Sample Size62
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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