A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696453



Internal ID15086419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:28324238..28467894hg38UCSC Ensembl
Innerchr8:28181755..28325411hg19UCSC Ensembl
Innerchr8:28237674..28381330hg18UCSC Ensembl
Innerchr8:28237674..28381330hg17UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg38143657
hg19143657
hg18143657
hg17143657
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518985
Supporting Variants
Samples
Known GenesFBXO16, PNOC, ZNF395
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696453
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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