A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7710n54



Internal ID18999886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:64094021..64095551hg38UCSC Ensembl
chr20:62725374..62726904hg19UCSC Ensembl
chr20:62195818..62197348hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg381531
hg191531
hg181531
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv586782, nsv586784, nsv586783, nsv586777
Samples
Known GenesOPRL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7710n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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