A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666106



Internal ID9932211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:38365610..38365928hg38UCSC Ensembl
Outerchr20:38365239..38366298hg38UCSC Ensembl
Innerchr20:36994266..36994572hg19UCSC Ensembl
Outerchr20:36993895..36994942hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg381060
hg191048
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5832659, essv5636515, essv5540229, essv5881095, essv5535665, essv6102434, essv6316381, essv6029234, essv6062604, essv5552141, essv5423773, essv6478010, essv5647160, essv5997957, essv5442499, essv6349854, essv5428140, essv6050515, essv6325916, essv5662006, essv5603657, essv5783665, essv6389619, essv6165861, essv5818959, essv5682521, essv6061541, essv6011166, essv6090126, essv5673433, essv6012872, essv6064607, essv5532743, essv6016231, essv6416850, essv5965448, essv6296712, essv5886056, essv6157319, essv5603962, essv6111194
SamplesHG01060, HG01173, HG01188, HG01066, HG00737, HG01051, HG01070, HG01168, HG00736, HG01083, HG01069, HG01080, HG01067, HG01170, HG01072, HG01176, HG01198, HG00637, HG01048, HG01183, HG01187, HG01171, HG00732, HG01095, HG01047, HG01102, HG01073, HG01197, HG01101, HG01107, HG01204, HG01075, HG01190, HG00734, HG01174, HG01108, HG01055, HG01082, HG01191, HG01061, HG00553
Known GenesLBP
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666106
Frequency
Sample Size1151
Observed Gain0
Observed Loss41
Observed Complex0
Frequencyn/a


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