A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4351n100



Internal ID22790438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:10536307..10775598hg38UCSC Ensembl
chr21:10736859..10976150hg19UCSC Ensembl
chr21:9758730..9998021hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38239292
hg19239292
hg18239292
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1064024, nsv1066547, nsv1064129
Samples
Known GenesTPTE
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4351n100
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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