A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2456e59



Internal ID22763676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:10744678..10814560hg38UCSC Ensembl
chr21:10697897..10767779hg19UCSC Ensembl
chr21:9719752..9789650hg18UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg3869883
hg1969883
hg1869899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3415327, esv3452097, esv3335620
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv2456e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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