A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv428251



Internal ID18624701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:21123596..21283701hg38UCSC Ensembl
Innerchr11:21145142..21305247hg19UCSC Ensembl
Innerchr11:21101718..21261823hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38160106
hg19160106
hg18160106
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv452060
SamplesNA19225
Known GenesNELL1
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)nsv428251
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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