A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv428219



Internal ID18277983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:70391353..70577619hg38UCSC Ensembl
Innerchr9:73006269..73192535hg19UCSC Ensembl
Innerchr9:72196089..72382355hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38186267
hg19186267
hg18186267
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv451757
SamplesHGDP00449
Known GenesKLF9, TRPM3
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)nsv428219
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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