A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660689



Internal ID9580108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:10433402..10433603hg38UCSC Ensembl
chr2:10573528..10573729hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38202
hg19202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5981660, essv5455988, essv6352210, essv5944362, essv5525652, essv6081972, essv5957322, essv5770788, essv6523675, essv6350837, essv5400840, essv6024922, essv6412423, essv6574658, essv5833555, essv5673368, essv6324956, essv5953662, essv5530933, essv5511442, essv5740929, essv5818620, essv6385519, essv5661119, essv5726289, essv5933313, essv6419723, essv5499585, essv5928379, essv6330230, essv6413203, essv5630300, essv6144387, essv6221273, essv6362933, essv5842581, essv5830991, essv5419670, essv5616961, essv5771241, essv5544702, essv6288514, essv5755722, essv6282130, essv6008158, essv5508491, essv5922483, essv6349831, essv6324644, essv6389231, essv6212479, essv6352045, essv5751801, essv5530367, essv5843675, essv6525364, essv5705166, essv5791549, essv5875436, essv6000695, essv5433137, essv6300173, essv5658551, essv6450525, essv5636828, essv6078941, essv5560100, essv6429243, essv6165575, essv6136866, essv5647192, essv5861273, essv5810315, essv6327911, essv6227917, essv5929833, essv6287220, essv5987766, essv5617771, essv6325221, essv5451816, essv5934801, essv5405973, essv6348846, essv6168049, essv6436659, essv5403735, essv5826737, essv5952172, essv6413682, essv6108151, essv6034444, essv5596146, essv5404952, essv6285895, essv5979371, essv6221319, essv5632509, essv6516492, essv5972584, essv6399567, essv6350758, essv5832288, essv6137567, essv5713626, essv6474205, essv5539761, essv6257935, essv5849282, essv6526592, essv5889758, essv6225466, essv5721016, essv5610597, essv5628615, essv6086703, essv5717282, essv6559476, essv6414430, essv5653928, essv6523735, essv6388102, essv6024392, essv6586988, essv6531756, essv6410438, essv6202568, essv5614352, essv5890651, essv6014336, essv5554475, essv6108515, essv6538256, essv6447347, essv6176146, essv5868457, essv5839085, essv5685095, essv6459201, essv5885144, essv5537012, essv6554289, essv5947142, essv5937113, essv5993675, essv5664884, essv6223060, essv5819877, essv6084753, essv5944879, essv5683290, essv5496237, essv6173220, essv6141382, essv5830565, essv6542297, essv5470465, essv5865189, essv6457119, essv6046635, essv6433468, essv5970769, essv5612479, essv5598558, essv6585773, essv5662074, essv6518906, essv6214132, essv6047563, essv6370458, essv6158234, essv6194474, essv5838136, essv6516482, essv5989618, essv5667223, essv6122004, essv6214680, essv6467811, essv6136531, essv5544887, essv6043235, essv5697745, essv5928729
SamplesHG00096, HG00114, NA19703, HG01462, HG00142, NA12286, NA20508, NA11995, NA18861, HG00187, NA19332, NA12414, NA20514, NA18507, HG01188, NA20813, NA20532, HG00367, NA19350, NA18486, NA19819, NA19777, NA20332, NA18959, HG00737, HG01518, NA20517, NA19443, NA19190, NA19920, NA12399, NA07357, HG00693, NA12413, NA20814, NA19374, NA19746, HG00127, NA19660, NA19319, NA19728, NA19448, HG01167, NA20774, HG01168, NA18923, NA20756, NA18567, NA20795, NA19916, HG00330, NA11918, HG00346, NA18582, HG01354, NA12287, HG01083, NA20513, NA19782, NA19681, NA19904, HG01134, HG00281, NA20759, NA20539, NA12282, NA12275, NA20518, NA19383, NA18874, NA20775, NA20812, NA11932, HG00232, NA19731, NA11994, NA19471, NA19317, NA12889, NA19722, NA20811, NA19901, HG00637, HG00338, NA20757, NA18908, HG00253, NA19921, NA19451, HG00108, NA12489, HG01360, HG00380, NA20787, HG01384, NA19403, HG00245, NA12342, NA20505, NA12003, NA19347, NA20809, NA18933, HG00732, NA20536, NA19717, NA18910, NA18871, HG00239, NA18548, HG01390, NA20525, NA19654, HG00324, NA19655, HG00117, NA18853, NA12827, NA19338, HG00144, HG00276, HG00152, NA19682, NA12144, NA20828, NA18523, NA19469, NA19318, NA20542, HG01107, HG01075, NA20799, NA19729, HG00476, NA20773, NA19390, NA11881, HG00285, NA19321, NA19108, NA19256, NA20276, NA19712, HG00353, NA20804, HG00278, NA19773, NA07051, NA12046, HG00308, NA20792, NA19439, NA20504, HG01137, NA20516, NA19360, NA20341, NA18501, NA19785, NA19438, NA19472, NA19060, NA19093, NA19102, NA19770, NA19726, NA11843, NA20826, NA19780, NA19213, NA19661, NA07056, NA18505, NA11892, NA19755, NA18488, NA19758, NA19312, NA12890, NA07000, NA18522, NA19429, NA18487, NA20772
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660689
Frequency
Sample Size1151
Observed Gain0
Observed Loss184
Observed Complex0
Frequencyn/a


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