A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4129e59



Internal ID22765349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38502177..38503775hg38UCSC Ensembl
chr8:38359695..38361293hg19UCSC Ensembl
chr8:38478852..38480450hg18UCSC Ensembl
Cytoband8p11.22
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 Variantsesv3346544, esv3357303
SamplesNA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4129e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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