A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv454624



Internal ID18620423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:131676282..131874112hg38UCSC Ensembl
Innerchr4:132597437..132795267hg19UCSC Ensembl
Innerchr4:132816887..133014717hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38197831
hg19197831
hg18197831
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428450
Supporting Variants
SamplesHGDP00476
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)nssv454624
Frequency
Sample Size62
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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