A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv428298



Internal ID18624748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24009191..24655767hg38UCSC Ensembl
Innerchr15:24254338..24900914hg19UCSC Ensembl
Innerchr15:21805431..22452007hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38646577
hg19646577
hg18646577
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv452617, nssv452629, nssv452619, nssv452618
SamplesHGDP01087, HGDP00450, NA19181, HGDP00449
Known GenesPWRN1, PWRN2
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)nsv428298
Frequency
Sample Size62
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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