A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv428168



Internal ID18624618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:105384366..105815622hg38UCSC Ensembl
Innerchr1:105926988..106358244hg19UCSC Ensembl
Innerchr1:105728511..106159767hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38431257
hg19431257
hg18431257
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv450853
SamplesNA19108
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)nsv428168
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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