A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520121



Internal ID8414396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:978696..1019141hg38UCSC Ensembl
Innerchr20:959339..999784hg19UCSC Ensembl
Innerchr20:907339..947784hg18UCSC Ensembl
Innerchr20:907339..947784hg17UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3840446
hg1940446
hg1840446
hg1740446
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697233
Samples
Known GenesRSPO4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
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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