A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700492



Internal ID15090458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:214984..583699hg38UCSC Ensembl
Innerchr8:164984..533699hg19UCSC Ensembl
Innerchr8:154984..523699hg18UCSC Ensembl
Innerchr8:154984..523699hg17UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg38368716
hg19368716
hg18368716
hg17368716
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524542
Supporting Variants
Samples
Known GenesFAM87A, FBXO25, RPL23AP53, TDRP, ZNF596
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700492
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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