A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669113



Internal ID9935218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:10939130..10939137hg38UCSC Ensembl
Outerchr10:10938980..10939283hg38UCSC Ensembl
Innerchr10:10981100..10981093hg19UCSC Ensembl
Outerchr10:10980943..10981246hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5855616, essv6433322, essv6001950, essv6050573, essv6251585, essv6534171, essv6136881, essv6304438, essv6305302, essv6354925, essv5803566, essv5681897, essv5627328, essv6581145, essv5988981, essv5581487, essv5703179, essv6304793, essv6414877, essv5916843, essv5712621, essv6135632, essv6075031, essv6033056, essv5888997, essv5554801, essv5980558, essv5933981, essv6405948, essv5644032, essv6303151, essv5425725, essv6422453, essv5825519, essv5488159, essv5462701, essv5794212, essv6387198, essv6321149, essv5559786, essv5708600, essv6430534, essv5820053, essv5879601, essv6561417, essv6334159, essv5600807, essv5960515, essv6337076, essv6541372, essv5890918, essv5567229, essv5834184, essv6297052, essv6374065, essv5721644, essv5746075, essv5787925, essv6321965, essv5675400, essv5452659, essv5527128, essv6372029, essv5580451, essv6389334, essv5610543, essv6305890, essv6108308, essv5987143, essv6499193, essv6146468, essv5498840, essv5543034, essv5859313, essv6171935, essv5776874, essv6114830, essv6347947, essv5532708, essv6399391, essv5635848, essv6304974, essv6256425, essv5901053, essv5924557, essv6046045, essv5462362, essv5756500, essv5427425, essv5627290, essv6079814, essv5842325, essv5570676, essv6577935, essv5530546, essv6500542, essv5799297, essv5710937, essv6222170, essv5647139, essv5607473, essv6182594, essv5811217, essv6310908, essv5798444, essv6211320, essv5786195, essv6039249, essv6085930, essv5733025, essv5888485, essv6457993, essv6137361, essv5559286, essv6558607, essv5714868, essv5774098, essv6031019, essv5862354, essv6102540, essv6102021, essv5882376, essv6212173, essv5894375, essv5986833, essv6223469, essv6255811, essv5847993, essv5493641, essv5458740, essv6405090, essv5439991, essv6454879, essv5494749, essv6067786, essv5987710, essv5638043, essv5987860, essv5622386, essv5935912, essv6387615, essv6228944, essv5969618, essv6134500, essv6273521, essv5409177, essv5669118, essv5568848, essv5907274, essv5568709, essv5969984, essv6352720, essv5622849, essv5698591, essv5622516, essv6487153, essv5948160, essv6477233, essv5984125, essv6374717, essv6440717, essv6390340, essv5463294, essv6177681, essv6582799, essv5487177, essv5504179, essv6378298, essv6411948, essv6288361, essv5697196, essv6226633, essv6015964, essv5557390, essv5715068, essv6314916, essv6094576, essv6363713, essv6469287, essv6003181, essv6459032, essv5791488, essv5750210, essv6073255, essv5436019, essv5639397, essv6156794, essv6565048, essv5531832, essv5408027, essv6585417, essv5842138, essv6025080
SamplesHG01441, HG00650, HG00542, HG00442, NA20543, HG00536, HG00608, NA18621, NA18947, HG00671, NA18592, HG00524, NA18561, NA12843, HG01188, NA20531, NA11933, HG00257, HG01389, HG01374, HG01066, HG00315, HG00699, NA19355, NA18530, NA18606, HG00449, HG00654, NA18526, HG01051, NA18633, HG00261, NA07357, NA18602, HG00337, HG00327, HG00663, NA19374, HG00138, NA19381, NA19373, HG01350, NA19379, NA18944, NA18940, NA18550, HG01070, HG00251, HG00501, NA18595, HG00702, HG00689, NA18619, HG00330, NA18547, NA11918, HG00346, NA18582, NA18571, HG01365, HG00537, HG00590, NA18611, HG00512, HG00139, NA20539, HG00277, HG01069, NA18977, HG01072, HG00232, HG00534, NA19385, HG00422, HG00705, NA19087, NA12889, HG00427, NA18557, HG00326, HG00323, HG00530, HG00419, NA18638, HG00464, HG01353, HG00543, HG00154, NA18605, NA18613, HG00443, HG01384, HG00557, HG00428, HG00653, NA18956, HG00701, HG00657, HG00475, HG00436, HG00556, HG00584, HG00533, HG00583, HG00344, NA18637, HG00500, HG00275, NA18572, NA18948, NA18534, HG00619, HG00708, HG00692, HG01390, HG00324, HG01073, NA18573, HG00651, NA20299, HG00250, HG00690, HG00531, HG00479, HG00684, HG01383, HG00613, HG01334, NA19009, NA18555, HG00276, HG00704, NA12144, HG00463, HG00246, NA18570, NA18546, NA18608, NA19375, HG00611, NA18542, NA12716, NA19390, HG00285, NA19147, NA18559, NA20276, NA18564, NA19072, HG00580, HG00375, HG00136, HG00278, NA07051, HG01357, HG01174, HG01375, HG00473, HG00607, NA19428, HG01108, HG00662, HG00418, HG00125, NA18501, HG00707, HG00672, HG00614, HG00111, HG00513, HG00421, HG00329, NA18636, NA18609, HG00310, HG00698, HG00343, NA18552, HG00252, HG01377, HG01378, HG00628, NA18624, NA12006, NA18623, NA18612, NA18549, NA18622, HG00437, NA18562, HG00581, NA18577, NA18620
Known GenesLINC00710
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669113
Frequency
Sample Size1151
Observed Gain0
Observed Loss193
Observed Complex0
Frequencyn/a


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