A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661753



Internal ID9581172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:107007869..107008251hg38UCSC Ensembl
chr11:106878595..106878977hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38383
hg19383
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6106419, essv6267796, essv5967856, essv6396245, essv6461977, essv5601751, essv6189844, essv5642460, essv6352724, essv5693216, essv5402787, essv5995663, essv5833255, essv5538329, essv6001416, essv5726836, essv5858947, essv5676492, essv5861811, essv5813452, essv6291819, essv5873236, essv5424022, essv5866829, essv5734653, essv5639841, essv5859069, essv6112745, essv5852440, essv5446054, essv5749832, essv6514876, essv5979207, essv6240371, essv5563393, essv6577092, essv5808297, essv6448663, essv6459199, essv5555975, essv5773935, essv6050835, essv5686934, essv6025587, essv5570287, essv6492954, essv5878366, essv6557653, essv5567037, essv5625667, essv5633078, essv5489128, essv6270986, essv6343779, essv5690255, essv6229224, essv5511574, essv5704391, essv5878094, essv6305736, essv6042202, essv6245837, essv6197811, essv6318880, essv5442855, essv6310562, essv5676536, essv6156058, essv6177254, essv6300250, essv6566462, essv6098463, essv5419305, essv6379683, essv6166130, essv5665278, essv6448062, essv5847754, essv5883199, essv6274750, essv6366818, essv6017436, essv6318695, essv6521735, essv5889233, essv6418514, essv6054481, essv6359835, essv6218104, essv5426594, essv6236246, essv5458280, essv5534085, essv6336109, essv5453705, essv5562322, essv5848494, essv6039827, essv6402737, essv6283607, essv5496492, essv5978727, essv5475996, essv5542406, essv5704494, essv5758861, essv5977692, essv6502262, essv6444136, essv6484019, essv6545302, essv5912099, essv6295301, essv6500316, essv6092726, essv6292424, essv6084192, essv6432916, essv5615843, essv6579229, essv5853136, essv6057396, essv5578682, essv6198528, essv5990986, essv6246219, essv5694156, essv5984431, essv5605149, essv5703154, essv6003639, essv6079341, essv6539493, essv6476659, essv5541903, essv5759389, essv5928316, essv5995267, essv6223961, essv6183761, essv5621411, essv6061806, essv6466114, essv5778930, essv6060474, essv6279807, essv5713328, essv6484429, essv5701765, essv6418537, essv5920414, essv5455032, essv5537789, essv6503531, essv5500987, essv5793499, essv5652432, essv5713269, essv5853131, essv6300737, essv6401489, essv5525456, essv6240973, essv6381806, essv5758683, essv5526556, essv6045072, essv6172546, essv5416392, essv5602341, essv6339288, essv6343205, essv6540956, essv5706965, essv5968470, essv6479798, essv5465162, essv6302803, essv5756401, essv6360584, essv5620291, essv5549141, essv5949964, essv5956022
SamplesHG01357, HG00613, NA19012, NA18964, HG00313, NA12043, HG00537, HG01359, HG00536, HG01440, HG01052, NA18561, NA18975, HG00437, NA18612, HG00731, HG00464, HG00596, NA19783, NA18526, HG00449, NA18550, NA18570, HG00707, NA18545, NA18603, NA18948, HG00463, HG00657, NA11931, NA18516, HG00614, HG01051, NA12813, HG00577, HG00475, NA19010, HG00375, HG00542, HG00326, NA18573, NA18542, HG01350, NA18541, NA18546, HG00701, HG00683, HG00698, HG00581, NA18963, NA19685, HG00404, HG01461, NA19678, HG00335, HG00578, HG00331, NA18965, HG00699, NA19780, HG00479, NA18596, NA19654, HG01133, NA18632, NA19762, HG00543, HG01107, NA19062, HG00339, HG00556, NA19067, NA12763, NA19085, NA18624, HG01140, NA18967, NA19054, NA19059, NA19076, HG00472, HG00421, HG00583, NA18566, HG01378, NA19057, NA18536, HG00638, NA18960, NA18990, HG00692, HG01495, NA19088, HG00628, HG00315, NA18638, NA18956, HG00533, NA18609, NA18976, NA18637, NA19075, HG00174, NA18982, NA19663, HG00276, HG00403, NA18634, NA19082, HG00584, HG01497, NA19000, NA19055, HG01111, NA19771, NA18572, HG00629, NA19716, NA18968, HG00559, NA19005, NA19657, HG00560, NA19731, NA18941, HG01356, HG00478, NA18564, NA18942, HG01351, NA18613, NA19720, NA18988, HG01060, NA18945, HG01149, NA19777, NA18987, NA18582, HG00427, NA18597, HG01095, HG00443, NA18599, NA18567, NA19078, NA19201, HG00611, NA18538, NA18565, NA18560, HG00580, NA18577, HG01390, NA18533, NA18548, NA19064, NA19770, NA19717, HG00656, HG00708, NA19070, HG00693, NA18611, HG00566, HG01498, HG00625, HG00690, HG00641, NA18532, NA18549, HG00442, HG00473, HG01377, NA18615, NA19758, HG00702, NA18555, NA19007, NA19661, NA19065, NA18980, HG01354, NA18553
Known GenesGUCY1A2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661753
Frequency
Sample Size1151
Observed Gain0
Observed Loss184
Observed Complex0
Frequencyn/a


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