A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4333n100



Internal ID22790420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:56895569..57105367hg38UCSC Ensembl
chr20:55470625..55680423hg19UCSC Ensembl
chr20:54904032..55113830hg18UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg38209799
hg19209799
hg18209799
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1063506, nsv1058289, nsv1064531
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4333n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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