A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4306n100



Internal ID20155922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37386619..37466486hg38UCSC Ensembl
chr20:36015022..36094888hg19UCSC Ensembl
chr20:35448436..35528302hg18UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3879868
hg1979867
hg1879867
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1060900, nsv1055212, nsv1059558, nsv1057519
Samples
Known GenesSRC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4306n100
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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