A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3468e59



Internal ID20130217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29806130..29904752hg38UCSC Ensembl
chr6:29773907..29872529hg19UCSC Ensembl
chr6:29881886..29980508hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3898623
hg1998623
hg1898623
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3384912, esv3354193
SamplesNA19240
Known GenesHLA-G, HLA-H
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv3468e59
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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