A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667322



Internal ID9586741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72064898..72065202hg38UCSC Ensembl
chr10:73824656..73824960hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38305
hg19305
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
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667322
Frequency
Sample Size1151
Observed Gain0
Observed Loss230
Observed Complex0
Frequencyn/a


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