A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4291n100



Internal ID22790378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:25682305..25764075hg38UCSC Ensembl
chr20:25662941..25744711hg19UCSC Ensembl
chr20:25610941..25692711hg18UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg3881771
hg1981771
hg1881771
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1056288, nsv1057618
Samples
Known GenesFAM182B, ZNF337
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4291n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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