A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520121



Internal ID6016055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:959339..999784hg19UCSC Ensembl
Innerchr20:907339..947784hg18UCSC Ensembl
Innerchr20:907339..947784hg17UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv697233
Samples
Known GenesRSPO4
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)nsv520121
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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