A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586772



Internal ID16027495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:64093902..64096125hg38UCSC Ensembl
Innerchr20:62725255..62727478hg19UCSC Ensembl
Innerchr20:62195699..62197922hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg382224
hg192224
hg182224
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv944468, nssv944467, nssv944463, nssv944464, nssv944466, nssv944469, nssv944465
Samples
Known GenesOPRL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586772
Frequency
Sample Size17421
Observed Gain6
Observed Loss1
Observed Complex0
Frequencyn/a


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