A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv452639



Internal ID18274795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28167321..28719643hg38UCSC Ensembl
Innerchr15:28412467..28964789hg19UCSC Ensembl
Innerchr15:26086062..26763830hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg38552323
hg19552323
hg18677769
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428299
Supporting Variants
SamplesNA19108
Known GenesGOLGA8F, GOLGA8G, GOLGA8M, HERC2, HERC2P9, MIR4509-1, MIR4509-2, MIR4509-3
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)nssv452639
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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