A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2465e59



Internal ID22763685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:10533078..10545076hg38UCSC Ensembl
chr21:10967381..10979379hg19UCSC Ensembl
chr21:9989252..10001250hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg3811999
hg1911999
hg1811999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3399426, esv3411211
SamplesNA19238, NA19240
Known GenesTPTE
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv2465e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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