A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518901



Internal ID15446194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:69323238..69342195hg38UCSC Ensembl
Innerchr8:70235473..70254430hg19UCSC Ensembl
Innerchr8:70398027..70416984hg18UCSC Ensembl
Innerchr8:70398027..70416984hg17UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg3818958
hg1918958
hg1818958
hg1718958
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696359
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518901
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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