A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586785



Internal ID16027508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:64094347..64095157hg38UCSC Ensembl
Innerchr20:62725700..62726510hg19UCSC Ensembl
Innerchr20:62196144..62196954hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38811
hg19811
hg18811
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv944499, nssv944500, nssv944497, nssv944501, nssv944498, nssv944496
Samples
Known GenesOPRL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586785
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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