A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv428363



Internal ID18624813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27242268..27414831hg38UCSC Ensembl
Innerchr19:27733176..27905739hg19UCSC Ensembl
Innerchr19:32425016..32597579hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38172564
hg19172564
hg18172564
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv453703
SamplesNA19181
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)nsv428363
Frequency
Sample Size62
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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