A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521784



Internal ID8416059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:81601175..81607703hg38UCSC Ensembl
Innerchr9:84216090..84222618hg19UCSC Ensembl
Innerchr9:83405910..83412438hg18UCSC Ensembl
Innerchr9:81445644..81452172hg17UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg386529
hg196529
hg186529
hg176529
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694553
Samples
Known GenesTLE1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
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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