A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv451367



Internal ID18620055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:215160..390422hg38UCSC Ensembl
Innerchr8:165160..340422hg19UCSC Ensembl
Innerchr8:155160..330422hg18UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg38175263
hg19175263
hg18175263
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428193
Supporting Variants
SamplesHGDP00463
Known GenesFAM87A, RPL23AP53, ZNF596
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)nssv451367
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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