A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662262



Internal ID9928367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:71265399..71267494hg38UCSC Ensembl
chr6:71975102..71977197hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg382096
hg192096
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6524765, essv6087096, essv6113332, essv6130906, essv6511750, essv5582806, essv5480023, essv5805280, essv5913241, essv5891926, essv6089474, essv5682487, essv6532074, essv5528011, essv5427434, essv6344805, essv6140074, essv6005639, essv6102498, essv6042572, essv6181945, essv5606483, essv5488570, essv6449775, essv6180052, essv5950275, essv5502589, essv5618070, essv5833129, essv6506337, essv5886862, essv6169538, essv5701097
SamplesHG01060, NA19700, NA20766, NA11829, HG00361, NA18508, NA18565, NA18999, NA19443, NA12813, HG00311, NA20291, NA20819, HG01170, NA20812, NA12044, HG01176, NA18908, HG00176, NA19403, NA19347, HG00732, NA20770, NA19064, NA19401, HG00638, NA19470, HG01108, NA20281, NA19468, HG01111, NA19312, HG01437
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662262
Frequency
Sample Size1151
Observed Gain0
Observed Loss33
Observed Complex0
Frequencyn/a


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