A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7703n54



Internal ID18999879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:64093085..64095411hg38UCSC Ensembl
chr20:62724438..62726764hg19UCSC Ensembl
chr20:62194882..62197208hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg382327
hg192327
hg182327
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv586754, nsv586756, nsv586743, nsv586744, nsv586757, nsv586755, nsv586742, nsv586736, nsv586751
Samples
Known GenesOPRL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7703n54
Frequency
Sample Size17421
Observed Gain63
Observed Loss16
Observed Complex0
Frequencyn/a


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