A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv451363



Internal ID18620588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:96943..261625hg38UCSC Ensembl
Innerchr8:46943..211625hg19UCSC Ensembl
Innerchr8:36943..201625hg18UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg38164683
hg19164683
hg18164683
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428193
Supporting Variants
SamplesHGDP00984
Known GenesOR4F21, 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)nssv451363
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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