A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3467e59



Internal ID20130216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29793867..29962582hg38UCSC Ensembl
chr6:29761644..29930359hg19UCSC Ensembl
chr6:29869623..30038338hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg38168716
hg19168716
hg18168716
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3426050, esv3411103
SamplesNA19240
Known GenesHCG4B, HLA-A, HLA-G, HLA-H, LOC554223
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv3467e59
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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