A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv609455



Internal ID16396864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:452692..570044hg38UCSC Ensembl
Innerchr8:402692..520044hg19UCSC Ensembl
Innerchr8:392692..510044hg18UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg38117353
hg19117353
hg18117353
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11809n54
Supporting Variantsnssv1102105
Samples
Known GenesFBXO25, TDRP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv609455
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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