A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv428202



Internal ID18624652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:82424481..82594872hg38UCSC Ensembl
Innerchr8:83336716..83507107hg19UCSC Ensembl
Innerchr8:83499271..83669662hg18UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38170392
hg19170392
hg18170392
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv451535
SamplesNA19113
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)nsv428202
Frequency
Sample Size62
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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