A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521784



Internal ID6019308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:84216090..84222618hg19UCSC Ensembl
Innerchr9:83405910..83412438hg18UCSC Ensembl
Innerchr9:81445644..81452172hg17UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv694553
Samples
Known GenesTLE1
Method
AnalysisCNV regions located outside of or spanning over several merged-level regions determined by the submitter
PlatformIllumina HumanHap550 Genotyping BeadChip v3
Comments
ReferenceShaikh et al 2009
Pubmed ID19592680
Accession Number(s)nsv521784
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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