A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3404e59



Internal ID20130153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:149202496..149204094hg38UCSC Ensembl
chr5:148582059..148583657hg19UCSC Ensembl
chr5:148562252..148563850hg18UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg381599
hg191599
hg181599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3375132, esv3414747, esv3383212
SamplesNA19239, NA19238, NA19240
Known GenesABLIM3
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv3404e59
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