A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2675056



Internal ID9941161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:123207815..123208374hg38UCSC Ensembl
chr11:123078523..123079082hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg38560
hg19560
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6393221, essv6089456, essv6302078, essv5960495, essv6381794, essv6552547, essv5484749, essv6369035, essv6103104, essv6033051, essv6181985, essv5566431, essv5751554, essv6237254, essv6258889, essv5412311, essv5728310, essv5511919, essv6277279, essv5933916, essv6565560, essv5930111, essv5605290, essv6058504, essv6483109, essv5520274, essv6198800, essv6142861, essv5877460, essv6092649, essv5470707, essv5504270, essv5861989, essv5610620, essv6168643, essv5817732, essv6565450, essv6328696, essv5533049, essv5406665, essv5591816, essv5954914, essv6004708, essv6234843, essv6338539, essv6201606, essv6546320, essv5784502, essv6507784, essv5795537, essv6088699, essv6255877, essv6088057, essv6278965, essv6591687, essv5775323, essv6457870, essv5958778, essv6571515, essv6570510, essv5593999, essv6585652, essv5454593, essv5835378, essv6545288, essv6464312, essv6490393, essv6273753, essv6112818, essv5837853, essv5952466, essv5518634, essv5774223, essv5700176, essv5649186, essv6255695, essv6436542, essv5399986, essv6387364, essv6191603, essv6205930, essv5712370, essv6252693, essv6021276, essv6369219, essv5540232, essv6522467, essv6075215, essv6448361, essv6075016, essv5989486, essv6274156, essv6441865, essv6445334, essv5519736, essv6388149, essv5543973, essv5471426, essv6046744, essv6499508, essv5992162, essv5874853, essv6285056, essv6476963, essv6463033, essv5757919, essv6529184, essv5713767, essv5754382, essv5462414, essv5484329, essv6140481, essv5725119, essv5748726, essv5422560, essv5677530, essv5602921, essv6230122, essv6064440, essv5458578, essv5870260, essv5834201, essv5658367, essv6333550, essv6535434, essv6181203, essv6071182, essv6342515, essv5553536, essv6126081, essv5814867, essv5568238, essv5776954, essv5808043, essv5979847, essv5989380, essv5731099, essv6369560, essv6458900, essv5666335, essv5800020, essv6033202, essv6075037, essv6018495, essv6144840, essv5907917, essv6423176, essv6270148, essv5424314, essv5917278, essv6461841, essv5462413, essv6109074, essv6038787, essv5728675, essv5458931, essv5725618, essv5795209, essv5887175, essv6453096, essv5575054, essv5612346, essv5565088, essv5603975, essv6595596, essv6035265, essv6514255, essv5690394, essv6327121, essv5843403, essv6582105, essv6259845, essv6431101, essv5718328, essv5837477, essv5979960, essv6072068, essv6564087, essv6086675, essv6574111, essv5924716, essv6563997, essv5414138, essv5559469, essv6373251, essv5492830, essv5853440, essv6530271, essv6141126, essv5851156, essv5660886, essv6083789, essv6054883, essv5978675, essv5849860, essv5665531, essv5757888, essv6497097, essv6224651, essv5785122, essv6315841, essv5535882, essv5502697, essv5645414, essv6057725, essv5924951, essv6431525, essv5687341, essv6291066, essv6570815, essv6550330, essv5805254
SamplesNA19676, HG01060, HG00189, HG01441, HG00650, NA12717, NA19648, HG01173, NA19700, HG01356, HG00143, HG00231, NA18924, NA18621, NA20766, NA18947, HG01079, NA11933, HG01389, HG01066, NA20802, NA20532, NA18917, HG00367, HG01465, HG00699, HG00103, NA20294, NA19777, NA12340, HG00566, NA19684, HG00737, NA18616, HG00449, NA20507, HG00261, NA20771, NA12399, NA18988, HG00337, HG00271, HG00663, NA20814, NA19374, HG01250, HG00641, NA19746, HG00127, NA18550, HG00122, NA19382, NA18597, NA20589, NA19678, HG01488, HG01168, NA18982, NA18635, NA18567, NA20795, NA18619, NA18960, HG00736, NA11992, HG01354, NA19313, HG01083, NA19054, NA20336, HG00537, HG00311, NA19404, HG00277, HG01455, HG01069, NA19651, HG01080, HG00120, HG00683, NA20819, HG01519, HG00236, NA19371, NA11994, NA18617, NA19385, NA18986, HG01440, NA19722, NA18520, HG01198, HG00637, HG01048, NA20342, NA19456, NA18638, HG00264, NA12748, HG00108, NA11831, HG01353, HG00137, HG00560, HG00731, NA19082, NA19670, NA18934, HG00328, HG00245, NA12342, HG00732, HG00653, NA20521, HG01095, HG00320, HG00344, HG00500, NA18910, HG01149, NA18534, NA20770, NA18630, HG00692, HG01047, HG01102, HG01094, NA20299, HG00373, NA11893, NA11894, NA18856, HG01383, NA19750, NA06989, HG00613, HG00321, HG00157, NA12827, HG01497, NA19761, HG00276, NA18963, NA19682, HG00463, NA12546, HG01204, NA19012, NA18608, NA20799, HG00611, HG00476, HG00124, NA19652, NA18542, NA19440, NA18535, HG00265, NA19147, NA18559, NA19434, HG00366, NA20815, HG00375, HG01551, HG00638, NA19773, NA20790, HG01375, HG00308, HG00607, NA19428, HG01137, HG00116, HG01108, NA19360, NA12763, HG00662, HG00418, NA19085, NA19818, NA19759, NA19078, HG00111, NA20348, HG00259, NA19779, HG00342, NA19716, HG01254, HG01055, HG00174, HG00123, HG00310, HG00186, HG00112, NA19726, NA20758, NA19900, HG00377, HG00372, HG01377, NA18989, NA19758, NA18623, HG01112, HG01097, HG00180, NA20754, NA19346, HG01437, HG00581
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2675056
Frequency
Sample Size1151
Observed Gain0
Observed Loss212
Observed Complex0
Frequencyn/a


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