A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3307e59



Internal ID22764527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:68964269..68966567hg38UCSC Ensembl
chr5:68260096..68262394hg19UCSC Ensembl
chr5:68295852..68298150hg18UCSC Ensembl
Cytoband5q13.1
Allele length
AssemblyAllele length
hg382299
hg192299
hg182299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3345357, esv3435534, esv3334736
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv3307e59
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