A curated catalogue of human genomic structural variation

Variant Details

Variant: esv2667322

Internal ID9586741
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72064898..72065202hg38UCSC Ensembl
chr10:73824656..73824960hg19UCSC Ensembl
Allele length
AssemblyAllele length
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5721878, essv5829676, essv6507111, essv5806699, essv5925201, essv6186317, essv6239219, essv5397740, essv6116678, essv6341222, essv5948687, essv6063690, essv6047360, essv6294460, essv6304343, essv5600146, essv5758756, essv5763182, essv5686033, essv6376642, essv6451964, essv6467315, essv6201816, essv5949770, essv6547638, essv5951041, essv6117725, essv6302856, essv6266677, essv6408371, essv6067349, essv6011489, essv6016470, essv5786518, essv5488526, essv5877782, essv5467332, essv5642587, essv5652554, essv5764449, essv5451795, essv5990165, essv6375328, essv6279319, essv5489735, essv5631648, essv5934461, essv6052602, essv5532458, essv5792000, essv5495272, essv6159961, essv5810145, essv5921159, essv5404395, essv6154350, essv6340468, essv6417428, essv6433124, essv6169876, essv6589034, essv6015454, essv6439515, essv5980272, essv6188626, essv5618324, essv5704819, essv5529755, essv5803464, essv5816109, essv5779267, essv5938421, essv5423366, essv5583855, essv5859256, essv5984271, essv6459980, essv5851950, essv6336264, essv6239724, essv5694680, essv5962216, essv5694065, essv6332138, essv6405206, essv6460011, essv6048095, essv5456698, essv5758222, essv5437933, essv5869205, essv6259391, essv5562237, essv6022033, essv6094434, essv6306320, essv5509817, essv6502629, essv6383373, essv5784121, essv5863102, essv5804033, essv5907821, essv5410234, essv5527594, essv5560440, essv5900961, essv6438986, essv5541214, essv5850290, essv6351577, essv6260233, essv5871658, essv5852457, essv6326318, essv5797018, essv6143419, essv6290518, essv5798294, essv5931329, essv5970240, essv6462927, essv6222134, essv5431239, essv5825858, essv5703497, essv6136727, essv5595849, essv5461018, essv6491295, essv6275340, essv6458371, essv6569535, essv5668723, essv6560106, essv5969443, essv6206895, essv6485022, essv6404618, essv6166131, essv6090909, essv6182836, essv6011470, essv6107773, essv6138689, essv5538506, essv6183794, essv5447916, essv5729335, essv5953884, essv6140460, essv6543920, essv6061932, essv5880475, essv5595997, essv5437432, essv6453955, essv6270859, essv6336439, essv6466344, essv5551679, essv5620868, essv6513045, essv5829485, essv5446347, essv5450140, essv5870347, essv6480528, essv5600474, essv6211977, essv5805205, essv6258106, essv5582504, essv5995552, essv5477331, essv5497498, essv5460694, essv5575095, essv5612568, essv6272325, essv5481972, essv5747941, essv5915737, essv5442400, essv5469148, essv5614042, essv6530863, essv6592724, essv6156529, essv6011379, essv5488594, essv5396869, essv5663287, essv5837222, essv5972090, essv5940383, essv6431661, essv5421748, essv6421677, essv6360024, essv6312232, essv6363826, essv5952682, essv6088244, essv6136729, essv6244526, essv5778160, essv6132864, essv6541612, essv5640814, essv5844116, essv5586348, essv6218208, essv5922375, essv5448416, essv5537954, essv6210317, essv6417310, essv6188976, essv6345962, essv6335718, essv5855182, essv5497204, essv5941886, essv5820479, essv6028577, essv6297712, essv5576547, essv5994269, essv6396229
SamplesHG00323, HG01441, NA18870, HG01515, HG00313, NA12043, NA19152, NA19625, HG01359, NA18861, HG00252, HG00318, HG01440, NA12750, HG00257, NA18616, HG00182, NA07037, NA18951, HG00344, NA18871, HG01072, HG01052, HG01075, NA18523, NA18952, NA18975, HG00500, HG00171, HG01083, NA20510, HG00112, HG00274, HG00731, HG00245, NA19311, HG00310, NA18570, HG00261, HG01079, NA10847, HG01389, NA18948, NA19430, HG01197, HG00657, NA18516, HG00614, HG01365, NA12813, HG01492, HG01082, NA12828, HG00475, HG00542, HG00173, HG00326, HG01491, NA19920, HG00270, HG00553, HG01350, NA18489, HG00190, NA19144, HG00122, NA18507, HG00683, HG00111, NA12776, NA19004, HG00335, NA19108, HG00331, HG00319, HG00253, NA12044, HG01171, HG00353, NA18596, HG00269, HG01133, NA18632, HG00342, HG00635, NA12414, HG00154, HG01107, HG00339, HG00158, HG00242, NA12763, HG00346, HG00250, NA18508, NA18967, NA19239, NA19059, NA11994, NA18536, HG00140, HG00638, HG00259, NA19443, NA07357, NA19444, HG01061, HG00231, HG00692, HG00689, NA12273, NA12761, NA18956, HG00338, NA18959, NA18609, HG00178, NA18547, HG00125, NA11831, NA18976, HG01136, NA11894, NA18637, NA18973, NA11995, NA18593, HG00243, HG00254, HG00276, HG00357, HG00237, HG00343, NA12144, HG00584, HG00114, NA12751, NA19190, HG00373, NA19725, HG00267, NA19377, HG01437, HG00124, NA07346, NA12892, NA19372, NA18572, NA19374, HG00268, HG00325, NA18968, NA19102, HG00263, NA06986, NA18510, HG00176, HG00260, NA18502, HG01073, NA18558, NA18977, NA19098, HG01170, HG01069, HG01356, NA18564, HG00116, HG00277, HG00740, NA19720, HG00329, HG01070, HG00246, NA19159, HG00377, NA18985, HG00236, HG00151, NA12891, NA18582, HG01137, HG00595, HG00443, NA06984, NA12156, NA19116, NA18989, NA18544, HG00311, NA18602, NA19818, HG01390, NA12878, NA19452, NA11830, HG00123, HG00285, NA18944, NA11993, NA19160, HG01366, HG01108, HG00367, NA19240, HG00320, HG00275, NA12717, NA18574, NA18853, NA19204, HG01374, HG00473, NA18981, NA19350, HG00137, HG01102, HG00684, NA06994, HG00143, NA19087, HG00272, HG00702, NA19200, HG00278, NA19007, NA07000, NA18980, HG00312, HG00327
Known GenesSPOCK2
AnalysisNo reference, merging analysis
Pubmed ID23128226
Accession Number(s)esv2667322
Sample Size1151
Observed Gain0
Observed Loss230
Observed Complex0

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