A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2042e59



Internal ID22763262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:2572273..2574471hg38UCSC Ensembl
chr2:2576045..2578243hg19UCSC Ensembl
chr2:2555052..2557250hg18UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg382199
hg192199
hg182199
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3395790, esv3348831, esv3445825
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv2042e59
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