A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv452550



Internal ID18274339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20389348..21014516hg38UCSC Ensembl
Innerchr15:20594601..21219845hg19UCSC Ensembl
Innerchr15:18854615..19484504hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38625169
hg19625245
hg18629890
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428296
Supporting Variants
SamplesHGDP01093
Known GenesCT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1, NF1P2, POTEB, POTEB2
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)nssv452550
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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