A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4345n100



Internal ID19014713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:64066107..64150343hg38UCSC Ensembl
chr20:62697460..62781696hg19UCSC Ensembl
chr20:62167904..62252140hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3884237
hg1984237
hg1884237
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1061184, nsv1055979
Samples
Known GenesC20orf201, MIR6813, NPBWR2, OPRL1, RGS19, TCEA2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4345n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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