A curated catalogue of human genomic structural variation

Variant Details

Variant: esv2675456

Internal ID9594875
Location Information
TypeCoordinatesAssemblyOther Links
chr11:113935087..113935460hg38UCSC Ensembl
chr11:113805809..113806182hg19UCSC Ensembl
Allele length
AssemblyAllele length
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5863727, essv5422232, essv5436188, essv6552068, essv5822984, essv5652610, essv5932659, essv5435407, essv5602206, essv5490819, essv5612401, essv5629383, essv6244166, essv5404836, essv6547297, essv5930155, essv6331604, essv6006406, essv6127353, essv6485835, essv6498753, essv6589096, essv5908805, essv5687157, essv6221708, essv6389142, essv6412300, essv5671116, essv6306306, essv5786807, essv5527884, essv5576722, essv5882840, essv6568606, essv5423061, essv5468764, essv6245131, essv5786036, essv5495896, essv5508309, essv5852330, essv6311044, essv5667316, essv5634537, essv5597768, essv5533406, essv6490271, essv5854132, essv6472283, essv6583419, essv5753038, essv6581108, essv5460651, essv5410681, essv6115192, essv5399402, essv5415430, essv5828554, essv6414040, essv5484610, essv5850577, essv6489161, essv6342156, essv5839710, essv6366713, essv5871282, essv6431142, essv5873531, essv5555660, essv5896302, essv6087485, essv6512892, essv5702080, essv5698162, essv5539784, essv5744148, essv6573827, essv6063630, essv5876707, essv5968283, essv6073070, essv5728621, essv5868210, essv6206286, essv5445980, essv5475820, essv6558137, essv5825395, essv6370551, essv5632483, essv6574894, essv5465873, essv6138242, essv5624134, essv5733192, essv5974187, essv6399925, essv5621938, essv6430819, essv5508694, essv5549789, essv6016594, essv6538827, essv5667833, essv6049388, essv5726207, essv5461804, essv5572588, essv5724284, essv6569001, essv6543775, essv5731618, essv5753006, essv5954012, essv6052982, essv6253954, essv6534448, essv6261310, essv5589846, essv6503374, essv5897302, essv5745593, essv5765751, essv5804465, essv5883490, essv6158574, essv5776962, essv6055292, essv6393473, essv5534493, essv6009804, essv5996381, essv5726969, essv6336195, essv6558378, essv6013241, essv6105247, essv5883868, essv6472765, essv6273116, essv5647526, essv5991363, essv5826921, essv5919183, essv5747837, essv6225472, essv6344900, essv6561794, essv6576712, essv5579964, essv6446718, essv5753271, essv5960292, essv6120848
SamplesNA18621, HG00309, HG00536, HG00607, NA07347, NA20787, NA19712, HG00257, NA18616, NA19904, NA18951, NA20522, HG00344, HG00100, HG00328, NA18523, HG00437, NA20516, HG00500, NA18612, NA20510, HG00112, HG00186, NA18550, NA18570, HG01079, NA20802, HG01389, NA11931, NA20808, NA18517, NA20529, HG00428, NA19920, NA20786, NA19782, HG01350, NA19461, NA18546, HG00683, HG00698, HG00581, NA18963, NA19648, HG00699, NA19780, NA19761, HG00353, NA19438, NA18632, NA20770, NA19077, HG00543, NA19062, NA20761, NA19067, NA20585, NA12843, NA19054, NA12282, HG00472, HG01378, NA11994, NA19068, NA12155, HG00180, NA18563, NA18618, HG01048, NA20530, HG01124, NA18592, NA18856, HG00533, NA20765, HG00125, HG00258, NA12829, NA20520, NA19773, NA18593, HG00284, NA19316, NA12751, HG00373, HG00620, NA12046, NA18620, NA18633, NA18572, HG00268, HG01066, NA12778, HG00325, NA20790, NA20753, NA19005, NA18558, HG00239, HG00501, NA20814, NA20818, NA20774, NA20828, NA18613, NA20542, NA18988, HG00512, NA19707, HG00525, NA18562, NA19789, NA18543, NA18619, NA18987, NA18582, NA20525, NA20537, HG00590, NA19376, NA18983, HG00650, NA19009, HG00663, NA18989, HG00580, HG00654, NA18548, NA11830, NA11992, NA12003, NA19064, HG00281, NA18944, NA18917, NA20758, HG00367, NA11932, NA11829, HG00625, HG00690, HG01374, HG01102, NA20524, NA20804, NA20806, HG00336, HG00671, HG00704, HG00271, NA07000, NA19466, NA18980, HG00361
Known GenesHTR3B
AnalysisNo reference, merging analysis
Pubmed ID23128226
Accession Number(s)esv2675456
Sample Size1151
Observed Gain0
Observed Loss154
Observed Complex0

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