A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4308n100



Internal ID19014676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38087420..38226717hg38UCSC Ensembl
chr20:36715822..36855119hg19UCSC Ensembl
chr20:36149236..36288533hg18UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38139298
hg19139298
hg18139298
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1061974, nsv1066774
Samples
Known GenesKIAA1755, RPRD1B, TGM2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4308n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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