A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668758



Internal ID9934863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:1703144..1704050hg38UCSC Ensembl
Outerchr2:1702773..1704420hg38UCSC Ensembl
Innerchr2:1706916..1707822hg19UCSC Ensembl
Outerchr2:1706545..1708192hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg381648
hg191648
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5487793, essv5559447, essv5402144, essv5822208, essv5580596, essv5660610, essv5690192, essv6298218, essv6086798, essv5790498, essv6577072, essv6469629, essv5474185, essv6492235, essv6213678, essv6008833, essv6275253, essv6315456, essv6259305, essv6065100, essv5585219, essv6338839, essv6296101, essv5562211, essv5469777, essv6098274, essv6417182, essv6372739, essv5567912, essv5654841, essv5579948, essv5690472, essv5785853, essv6096922, essv5931268, essv5659907, essv5455384, essv5412060, essv6571299, essv6147653, essv5656043, essv5565424, essv5563699, essv5842346, essv6412710, essv5901095, essv6037057, essv6498769, essv6299518, essv6145374, essv5882910, essv5870839, essv6418545, essv5841635, essv6542828, essv6284826, essv5995563, essv5940617, essv6130784, essv5715033, essv6199828, essv5730058, essv6050490, essv5843942, essv6350436, essv5521496, essv6296770, essv6055560, essv6286755, essv6228886, essv5897635, essv6446887, essv5866314, essv6547603, essv6321356, essv6079916, essv5504877, essv5628182, essv5816283, essv5977241, essv5955165, essv5888445, essv6407873, essv6303544, essv6457611, essv6031464, essv6566622, essv5405994, essv5534736, essv5825829, essv6567358, essv5462940, essv5451274, essv5955698, essv6576201, essv6430193, essv5464656, essv6463605, essv6587028, essv6179158, essv5797787, essv6442853, essv5910636, essv5940509, essv6380454, essv6519380, essv6228535, essv5962725, essv5664610, essv6584203, essv5735782, essv5415659, essv6058669, essv6052407, essv5399672, essv5992613, essv5693316, essv6404948, essv6376485, essv6000099, essv6173309, essv6404937, essv6507790, essv6020610, essv5621691, essv6532922, essv6195509, essv6234195, essv6153573, essv6356596, essv5858535, essv6161712, essv5915207, essv6257233, essv5579315, essv6362030, essv5994562, essv5495310, essv5790698, essv6394485, essv5489442, essv6523415, essv6429598, essv6483984, essv6383936, essv5847859, essv5670398, essv6462774, essv6328372, essv5612349, essv5416915, essv5863771, essv6380729, essv6214655, essv5806222, essv5730862, essv6491458, essv5936601, essv5825816, essv5699608, essv5783671, essv6493948, essv5613498, essv6191707, essv5728987, essv5782791, essv5958443, essv5537441, essv6082019, essv6564325, essv6550164, essv6112725, essv5961662, essv5686648, essv6009571, essv5659877, essv6344330, essv6213646, essv5980583, essv5449828, essv5643359, essv6136569, essv5666299, essv5871676, essv6010875, essv5471444, essv6209855, essv6038171, essv5596961, essv5875551, essv6065883, essv6286604, essv6513267, essv6269264, essv6495213, essv6027083, essv5659720, essv5584770, essv5725926, essv6560153, essv5803702, essv5799557, essv5656104, essv6365134, essv6059119, essv5852914
SamplesNA20588, HG01441, NA20529, NA20543, HG01462, NA20766, NA20508, HG00361, HG00242, NA20783, HG01079, NA20514, HG01188, NA20531, HG01389, HG01374, HG01066, HG00315, HG00306, HG00151, NA20816, NA20813, NA20752, NA20802, NA20532, NA20512, HG00640, HG00367, HG01465, HG00699, NA19819, NA19393, NA20805, NA12340, NA18530, NA20517, NA20507, HG01461, NA20771, NA20806, HG01140, NA12341, NA20814, NA20537, HG00641, HG01350, NA20796, HG01070, HG00589, NA20798, NA20589, HG01351, NA18595, NA19678, HG01488, NA20586, NA19723, NA18635, NA20756, HG01492, NA07048, HG01354, NA20768, NA20540, HG01083, HG00247, NA20513, NA19130, NA20541, HG01134, NA20759, NA20539, NA12275, HG01080, HG01067, NA20518, NA18874, NA20819, NA20775, HG01170, NA20812, NA18977, NA18868, NA19385, NA19002, NA20811, NA18990, HG01198, HG00637, HG00338, HG01048, HG01133, NA19456, NA20757, NA18867, NA20515, NA20753, HG01124, NA20818, NA18614, HG00313, HG01136, NA20535, NA20800, HG00176, NA20787, NA20524, HG00245, NA20505, NA19462, HG00190, NA20809, HG00732, NA20521, NA20810, NA20760, NA20536, NA19717, NA19663, HG00583, NA19081, NA20506, NA12718, NA20519, NA20126, NA20770, HG01390, NA20525, HG01102, NA19461, NA20581, HG01197, HG00331, NA20538, HG00276, HG00704, NA18523, HG00463, NA20542, NA18634, NA12546, HG01107, NA20534, NA19675, NA20765, NA20526, HG01148, NA20799, HG00476, NA20773, NA20522, NA20801, NA20815, NA18950, HG00357, HG00734, HG00136, NA20804, NA20520, NA20785, NA19010, HG01357, HG01174, NA20790, NA20530, NA20527, NA20792, NA20778, NA20504, NA20544, HG01137, NA20516, NA20803, NA18615, HG01489, NA19078, HG00707, HG01491, NA19438, NA20582, HG00421, HG00329, HG00342, HG00267, HG01055, HG00123, NA20510, NA20807, HG00280, NA20758, NA20826, NA19711, NA19213, NA20528, NA18983, HG00274, NA20503, NA20502, NA18984, HG01125, HG00171, NA20585, HG00554, NA20754, NA19431, NA20509
Known GenesPXDN
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668758
Frequency
Sample Size1151
Observed Gain0
Observed Loss206
Observed Complex0
Frequencyn/a


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