A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521360



Internal ID15448653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:25152990..25171156hg38UCSC Ensembl
Innerchr8:25010505..25028671hg19UCSC Ensembl
Innerchr8:25066422..25084588hg18UCSC Ensembl
Innerchr8:25066422..25084588hg17UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3818167
hg1918167
hg1818167
hg1718167
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697970
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521360
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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