A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3709e59



Internal ID22764929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166285398..166285821hg38UCSC Ensembl
chr6:166698886..166699309hg19UCSC Ensembl
chr6:166618876..166619299hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38424
hg19424
hg18424
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3400907, esv3390013
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
SOLiD
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv3709e59
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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