A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv428218



Internal ID18277982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:68226146..68427183hg38UCSC Ensembl
Innerchr9:70841062..71042099hg19UCSC Ensembl
Innerchr9:70030882..70231919hg18UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg38201038
hg19201038
hg18201038
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv451756
SamplesNA19189
Known GenesCBWD3, CBWD5, FOXD4L3, PGM5, PGM5-AS1
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)nsv428218
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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