A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1106e199



Internal ID6312210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32514445..32563492hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg19n/a
Variant TypeCNV Deletion
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsesv2665380, esv2677681
SamplesHG00734, HG01518, HG01072, HG01052, HG01519, HG01075, HG01055, HG01083, HG00731, HG01098, HG01079, HG01197, HG01051, HG01082, HG01174, HG00553, HG01182, HG01167, HG01188, HG01204, HG01101, HG01168, HG00737, HG01171, HG00554, HG01521, HG01107, HG00638, HG01048, HG01061, HG01183, HG00637, HG01187, HG01097, HG01516, HG01191, HG00640, HG01066, HG00732, HG01073, HG01170, HG01069, HG01176, HG01080, HG01070, HG01060, HG01190, HG01095, HG01108, HG01522, HG01102, HG01067, HG01198
Known GenesHLA-DRB1, HLA-DRB6
Method
Analysis
Platform
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1106e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss53
Observed Complex0
Frequencyn/a


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