A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4369n100



Internal ID22790456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:10338676..10552044hg38UCSC Ensembl
chr21:10960413..11173781hg19UCSC Ensembl
chr21:9982284..10195652hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38213369
hg19213369
hg18213369
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1059574, nsv1057718, nsv1057112, nsv1058148, nsv1065591, nsv1062471, nsv1061547, nsv1055208, nsv1056624, nsv1060170, nsv1058358, nsv1063919, nsv1059237, nsv1065257
Samples
Known GenesBAGE, BAGE2, BAGE3, BAGE4, BAGE5, TPTE
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4369n100
Frequency
Sample Size11257
Observed Gain48
Observed Loss0
Observed Complex0
Frequencyn/a


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