A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586806



Internal ID16027529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:64094816..64095271hg38UCSC Ensembl
Innerchr20:62726169..62726624hg19UCSC Ensembl
Innerchr20:62196613..62197068hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38456
hg19456
hg18456
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv944539
Samples
Known GenesOPRL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586806
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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