A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7706n54



Internal ID18999882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:64093345..64096125hg38UCSC Ensembl
chr20:62724698..62727478hg19UCSC Ensembl
chr20:62195142..62197922hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg382781
hg192781
hg182781
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv586747, nsv586761
Samples
Known GenesOPRL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7706n54
Frequency
Sample Size17421
Observed Gain13
Observed Loss0
Observed Complex0
Frequencyn/a


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