A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669899



Internal ID9589318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90841444..90842179hg38UCSC Ensembl
chr9:93603726..93604461hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg38736
hg19736
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5853172, essv6058075, essv5916716, essv5865625, essv6275493, essv5710827, essv6403724, essv5652868, essv5596056, essv5857766, essv5528325, essv6391555, essv5972310, essv5953476, essv5569753, essv5844304, essv6015773, essv6154685, essv5554608, essv6206021, essv5800647, essv5935257, essv5664982, essv5407488, essv6374181, essv5728604, essv5794704, essv6222347, essv6313686, essv5550615, essv5709323, essv5759417, essv6079961, essv5650463, essv5689862, essv6106776, essv6290486, essv5654705, essv5991721, essv5430754, essv5660131, essv5898792, essv5970029, essv5977601, essv6327584, essv6503995, essv5601660, essv5440988, essv5506587, essv5534139, essv6251431, essv6371466, essv5939532, essv5616346, essv5861463, essv5548342, essv5825761, essv5869606, essv6109613, essv6472571, essv6439118, essv6081111, essv6261326, essv5867954, essv5664876, essv5514994, essv6258588, essv6277011, essv6552982, essv6447808, essv5503329, essv6393269, essv6155138, essv5799085, essv5860773, essv6074985, essv6490968, essv6513587, essv5693370, essv6051795, essv6351664, essv6398340, essv5543579, essv5427046, essv6479978, essv5888861, essv5874977, essv6531655, essv5634980, essv5428797, essv6303295, essv6186491, essv6305785, essv6150177, essv6262287, essv6444845, essv5463634, essv5762858, essv5431426, essv6526737, essv5929383, essv6511643, essv5675749, essv5739075, essv5513236, essv6104578, essv5983150, essv6316273, essv6175236, essv6389944, essv6443387, essv5646881, essv6598193, essv6273819, essv6517893, essv5749169, essv6093156, essv6040862, essv6361364, essv5419557, essv5814200, essv5954779, essv5826722, essv5855031, essv6417999, essv5453166, essv5637126, essv5560845, essv6227463, essv6444720, essv6493609, essv5749987, essv6269511, essv5423704, essv5532860, essv5812868, essv6150493, essv6516387, essv6220171, essv5849812, essv5982055, essv6331725, essv5560671, essv5772919, essv6190604, essv6446459, essv5724190, essv5573188, essv6370033, essv6066029, essv5607638, essv6264862, essv5586072, essv6465356, essv5555304, essv6499625, essv6200621, essv5781037, essv5581248, essv6488577, essv6544273, essv5482673, essv5884817, essv5477044, essv6453887, essv5609129, essv6161891, essv6374995, essv6366402, essv5660084, essv6518104, essv5620648, essv5569322, essv6341981, essv5779146, essv6008716, essv5544316, essv5787517, essv6335326, essv5783592, essv5868623, essv6081216, essv6516217, essv5808883, essv6119764, essv6223134, essv6077166, essv5641273, essv5696193, essv6210548, essv6561352, essv6144784, essv5466785, essv5493264, essv6437398, essv5510053, essv6417802, essv5851340, essv6217812, essv6236351, essv6365755, essv5701422, essv5756021, essv5738574, essv6375017
SamplesNA20588, NA12383, NA19701, NA12717, HG01173, NA19700, NA20543, NA19909, HG00249, HG00671, NA20783, NA19332, NA20514, HG01374, HG01066, HG00315, NA20813, NA18999, NA20802, NA12045, HG00318, NA19393, NA20332, NA18530, NA12058, NA18959, NA18606, NA20808, NA18616, HG00449, NA20517, NA19443, NA19920, HG01522, HG01140, NA12413, NA12341, HG00337, NA19107, NA07346, NA19373, NA20796, HG00501, NA19382, NA20798, NA19678, NA20586, NA19723, NA18982, NA18635, NA18567, NA20795, HG00330, NA20769, NA19649, NA19062, NA07048, NA07347, HG00346, HG01083, NA19054, HG00270, HG01365, HG00311, NA20541, HG01134, NA12275, NA19651, NA20278, HG00106, NA20775, NA20812, NA18977, NA18868, HG00325, HG00262, NA18560, NA18617, HG00705, HG00182, HG00427, NA19901, NA19189, NA18990, NA18520, NA12828, NA20757, NA18908, HG00253, NA19921, NA19451, HG00264, HG00108, HG01124, HG00260, HG00137, HG00133, HG01136, HG00154, NA18605, NA19210, NA20800, HG00380, HG00282, NA19056, NA20524, NA19403, HG00328, NA19077, NA20809, HG00653, NA20521, NA20810, NA20760, NA20536, HG00368, HG00320, HG00583, NA19788, NA20506, NA18910, NA18572, NA18534, NA19776, NA19064, HG00740, HG01047, HG00284, HG01073, HG00250, HG00373, NA20581, NA12829, HG00157, HG01334, NA19338, NA18555, HG00146, HG00704, NA20828, NA19756, HG00141, NA18536, NA18634, NA19675, NA18945, NA18541, NA19012, NA19685, HG00155, NA18535, NA11881, NA19712, HG00353, NA19473, NA18628, NA20815, NA19072, HG00734, NA19010, NA20790, NA20527, NA20792, NA20778, NA19324, NA19467, HG00116, HG01108, NA20803, HG00256, NA19783, NA19085, NA06986, NA19818, NA19078, NA20348, NA19248, NA19472, NA19060, HG00329, HG00342, NA19713, NA20786, HG00698, NA11843, NA20758, NA20826, NA19213, NA19900, HG00372, HG00252, HG00147, NA07056, NA18989, NA11892, NA18488, NA19312, NA20322, NA07000, HG00554, NA18549, NA19429, HG01061, NA18577, NA20772
Known GenesSYK
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669899
Frequency
Sample Size1151
Observed Gain0
Observed Loss205
Observed Complex0
Frequencyn/a


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