A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1106e199



Internal ID22758879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32546668..32595715hg38UCSC Ensembl
chr6:32514445..32563492hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3849048
hg1949048
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2677681, esv2665380
SamplesHG01060, HG01521, HG01098, HG01052, HG01079, HG01188, HG01066, HG00640, HG00737, HG01518, HG01051, HG01522, HG01070, HG01167, HG01168, HG01083, HG01069, HG01080, HG01067, HG01519, HG01170, HG01072, HG01176, HG01198, HG00637, HG01048, HG01183, HG00731, HG01187, HG01171, HG00732, HG01095, HG01102, HG01073, HG01197, HG01182, HG01101, HG01107, HG01204, HG01075, HG01190, HG00734, HG00638, HG01174, HG01108, HG01055, HG01082, HG01097, HG00554, HG01191, HG01061, HG00553, HG01516
Known GenesHLA-DRB1, HLA-DRB6
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
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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