A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv454573



Internal ID18621030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:114085964..114254068hg38UCSC Ensembl
Innerchr4:115007120..115175224hg19UCSC Ensembl
Innerchr4:115226569..115394673hg18UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38168105
hg19168105
hg18168105
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428448
Supporting Variants
SamplesHGDP01093
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)nssv454573
Frequency
Sample Size62
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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