A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2046e59



Internal ID22763266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:3109673..3111171hg38UCSC Ensembl
chr2:3113445..3114943hg19UCSC Ensembl
chr2:3092452..3093950hg18UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg381499
hg191499
hg181499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3432247, esv3425840, esv3330806
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv2046e59
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