A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661060



Internal ID9927165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:112254528..112254642hg38UCSC Ensembl
Outerchr11:112254489..112254699hg38UCSC Ensembl
Innerchr11:112125251..112125365hg19UCSC Ensembl
Outerchr11:112125212..112125422hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg38211
hg19211
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6598154, essv5814601, essv5640667, essv6580061, essv6429231, essv6203131, essv6072941, essv6445124, essv5509447, essv5537082, essv5808765, essv5527551, essv6520376, essv6084747, essv5721520, essv6181400, essv5449811, essv6242720, essv5508448, essv6293920, essv5774574, essv6424744, essv6029028, essv5681672, essv5508423, essv6481457, essv6458508, essv6121054, essv5810336, essv5604939, essv5925157, essv5424851, essv5741105, essv6330026, essv5990425, essv5608855, essv5607950, essv5987896, essv5967433, essv5977939, essv5614180, essv5533071, essv6355584, essv5915831, essv6155401, essv6274853, essv5571265, essv6216203, essv5610066, essv5575863, essv5416325, essv6097025, essv6037891, essv5896350, essv5618508, essv6444327, essv5978375, essv6167881, essv5698097, essv6466562, essv6034039, essv5947824, essv6364829, essv6437620, essv6216411, essv6083701, essv6428013, essv6005587, essv5619052, essv6593251, essv5798486, essv6229385, essv5833747, essv6078988, essv6017926, essv6516062, essv6292718, essv5828579, essv5934053, essv5610943, essv5883693, essv6386928, essv5859229, essv5761846, essv5712893, essv5442153, essv6475316, essv5637193, essv5573932, essv5628362, essv5454132, essv5773903, essv6232066, essv6016746, essv5649809, essv5440953, essv5971509, essv5428647, essv6346317, essv5770890, essv5625210, essv5560862, essv5510988, essv6555595, essv6036266, essv5811719, essv5681976, essv6315080, essv5737091, essv5967837, essv5428237, essv5897853, essv5686734, essv6384414, essv5971157, essv5497168, essv5704914, essv5506975, essv6281930, essv5839713, essv5801692, essv5528585, essv5675748, essv6110598, essv5895227, essv6206013, essv6169947, essv5689948, essv6115992, essv5696840, essv6515306, essv6500600, essv6467890, essv6356823, essv5803467, essv5654867
SamplesNA12383, NA19648, NA12842, NA19703, NA18947, NA12286, NA20783, NA20514, NA12843, NA20816, NA20813, NA20802, NA20532, NA18545, NA19819, NA20805, NA18530, NA20808, NA18616, HG00150, NA20507, NA19920, NA18633, NA20771, NA12399, NA20806, NA19067, NA18988, NA12413, NA20537, NA07346, NA19660, NA20796, NA18944, NA18940, NA18595, NA19678, HG00448, NA20774, NA18635, NA18567, NA20795, NA20769, NA12348, NA19062, NA18574, NA12283, NA20768, NA19457, NA20513, NA19904, NA11930, NA20819, NA20775, NA06984, NA20812, NA11932, HG00232, HG00534, HG00309, NA20811, NA20757, NA20533, HG00323, NA18638, NA20818, NA19007, HG00137, NA18544, NA18605, NA20800, NA19056, NA20787, NA12342, NA20505, NA19347, NA20521, NA18956, NA20810, NA20760, NA20536, NA19717, NA20770, NA18573, HG00479, NA20581, NA18856, NA12827, HG00146, NA18963, NA20828, NA12778, NA19012, NA18576, NA20765, NA19003, NA20799, NA20773, NA18535, NA12775, NA20815, NA19732, NA20804, NA20785, NA19010, NA20790, NA18943, NA20803, NA20797, NA07037, NA12347, HG00339, NA19376, HG00111, NA18987, NA19474, NA12830, HG00186, NA20786, NA20807, NA20758, NA20826, NA19213, NA20503, NA19661, NA20502, NA11892, NA19004, NA18488, NA12890, NA18612, NA19429, NA18622, NA18562, NA18577, NA18620
Known GenesPLET1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661060
Frequency
Sample Size1151
Observed Gain0
Observed Loss136
Observed Complex0
Frequencyn/a


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