A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv428237



Internal ID18624687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:105839536..105993781hg38UCSC Ensembl
Innerchr10:107599294..107753539hg19UCSC Ensembl
Innerchr10:107589284..107743529hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38154246
hg19154246
hg18154246
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv451952, nssv451951, nssv451950
SamplesNA18916, NA19113, NA19147
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)nsv428237
Frequency
Sample Size62
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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