A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517882



Internal ID15445175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:84514467..84564308hg38UCSC Ensembl
Innerchr9:87129382..87179223hg19UCSC Ensembl
Innerchr9:86319202..86369043hg18UCSC Ensembl
Innerchr9:84358936..84408777hg17UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3849842
hg1949842
hg1849842
hg1749842
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv489n21
Supporting Variantsnssv695290
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517882
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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