A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv452845



Internal ID18273969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:99695998..100216834hg38UCSC Ensembl
Innerchr15:100236203..100757039hg19UCSC Ensembl
Innerchr15:98053726..98574562hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38520837
hg19520837
hg18520837
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428313
Supporting Variants
SamplesHGDP00986
Known GenesADAMTS17, DNM1P46, LYSMD4, MEF2A
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)nssv452845
Frequency
Sample Size62
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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