A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv450137



Internal ID18620860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:131676282..132009571hg38UCSC Ensembl
Innerchr4:132597437..132930726hg19UCSC Ensembl
Innerchr4:132816887..133150176hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38333290
hg19333290
hg18333290
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428450
Supporting Variants
SamplesHGDP01088
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)nssv450137
Frequency
Sample Size62
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer