A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524542



Internal ID15105149
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 StatusM
Merged Variants
Supporting Variantsnssv700492
Samples
Known GenesFAM87A, FBXO25, RPL23AP53, TDRP, ZNF596
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524542
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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