A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4303n100



Internal ID20155919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35730307..35805624hg38UCSC Ensembl
chr20:34318229..34393546hg19UCSC Ensembl
chr20:33781643..33856960hg18UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3875318
hg1975318
hg1875318
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1061972, nsv1059694, nsv1067494
Samples
Known GenesPHF20, RBM39
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4303n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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