A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519796



Internal ID6014408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:75782131..75784327hg19UCSC Ensembl
Innerchr9:74971951..74974147hg18UCSC Ensembl
Innerchr9:73011685..73013881hg17UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnssv689256, nssv658757
Samples
Known GenesANXA1
Method
AnalysisMerged-level CNV regions
PlatformIllumina HumanHap550 Genotyping BeadChip v3
Comments
ReferenceShaikh et al 2009
Pubmed ID19592680
Accession Number(s)nsv519796
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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