A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv452811



Internal ID18273350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:84046870..84599651hg38UCSC Ensembl
Innerchr15:84715622..85142882hg19UCSC Ensembl
Innerchr15:82506626..82943886hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38552782
hg19427261
hg18437261
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428310
Supporting Variants
SamplesHGDP00463
Known GenesDNM1P41, EFTUD1P1, GOLGA6L4, GOLGA6L5P, LINC00933, LOC100505679, LOC388152, LOC440300, LOC642423, UBE2Q2P1
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)nssv452811
Frequency
Sample Size62
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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