A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669752



Internal ID9935857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:22896398..22896591hg38UCSC Ensembl
chr6:22896627..22896820hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38194
hg19194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6598152, essv5852044, essv6318259, essv5955569, essv5621759, essv5750040, essv5629923, essv6374534, essv6517938, essv5407410, essv6551079, essv6437542, essv6156916, essv5778911, essv6352715, essv6583437, essv6142468, essv5501028, essv6493548, essv6346813, essv5724673, essv6281516, essv6552800, essv6502086, essv6450853, essv5849956, essv5503556, essv6160619, essv5552806, essv5970345, essv5847454, essv5692906, essv5540328, essv5562553, essv6041699, essv5577482, essv6491744, essv5951173, essv6179461, essv6442779, essv5971293, essv6461489, essv6293519, essv5957748, essv6129489, essv6049020, essv6396131, essv6176910
SamplesNA18508, NA19399, NA20332, NA19377, NA19190, NA18870, NA19920, HG00261, HG00693, NA19374, NA19373, NA20589, NA19198, NA19384, NA20278, NA19383, NA19371, NA19235, HG01048, NA20342, NA12828, NA18867, NA19437, HG01171, HG00282, NA18933, NA19391, NA19461, NA19469, NA19436, NA19401, NA19375, NA11881, NA19147, NA20815, NA19435, HG01174, HG00237, NA20281, NA20341, NA19376, NA18501, NA19213, HG00252, NA18505, NA19312, NA19429, NA18487
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669752
Frequency
Sample Size1151
Observed Gain0
Observed Loss48
Observed Complex0
Frequencyn/a


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