A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677681



Internal ID9943786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32547039..32584345hg38UCSC Ensembl
Outerchr6:32546668..32584715hg38UCSC Ensembl
Innerchr6:32514816..32552122hg19UCSC Ensembl
Outerchr6:32514445..32552492hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3838048
hg1938048
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1106e199
Supporting Variantsessv6407181, essv5705308, essv6046230, essv5561530, essv5806408, essv5725752, essv6236871, essv5682167, essv5450725, essv6525435, essv5680302, essv5446928, essv5448093, essv6119008, essv6080374, essv6362148, essv5800490, essv5493556, essv6159442, essv6306341, essv6158263, essv6242831, essv6510792, essv6059394, essv5767209, essv6524238, essv5791822, essv6549425, essv5719476, essv5877372, essv6253057, essv5399875, essv6552563, essv5619702, essv5891896, essv5620801, essv5596059, essv6267418, essv6270210, essv6009671, essv5859647, essv6594361, essv6397431, essv5493329, essv6249416, essv6434861, essv5623120, essv6331554
SamplesHG01060, HG01098, HG01052, HG01079, HG01188, HG01066, HG00640, HG00737, HG01051, HG01070, HG01167, HG01168, HG01083, HG01069, HG01080, HG01067, 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
Known GenesHLA-DRB1, HLA-DRB6
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677681
Frequency
Sample Size1151
Observed Gain0
Observed Loss48
Observed Complex0
Frequencyn/a


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