A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv451734



Internal ID18274831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:65584075..65758917hg19UCSC Ensembl
Innerchr9:65323895..65498737hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg19174843
hg18174843
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428215
Supporting Variants
SamplesNA19113
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)nssv451734
Frequency
Sample Size62
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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