A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv453601



Internal ID18620447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:78264380..78768164hg38UCSC Ensembl
Innerchr18:76024380..76528164hg19UCSC Ensembl
Innerchr18:74125368..74629152hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38503785
hg19503785
hg18503785
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428358
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)nssv453601
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