A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2463e59



Internal ID22763683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:10565678..10578176hg38UCSC Ensembl
chr21:10934281..10946779hg19UCSC Ensembl
chr21:9956152..9968650hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg3812499
hg1912499
hg1812499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3381401, esv3451293, esv3399311
SamplesNA19238, NA19239, NA19240
Known GenesTPTE
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv2463e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer