A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671782



Internal ID9937887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:92872305..92872441hg38UCSC Ensembl
Outerchr9:92872148..92872594hg38UCSC Ensembl
Innerchr9:95634587..95634723hg19UCSC Ensembl
Outerchr9:95634430..95634876hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38447
hg19447
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5687589, essv5538142, essv5656456, essv5711647, essv5661831, essv5811692, essv6324121, essv5889825, essv6313191, essv5401017, essv5932371, essv6000736, essv5652191, essv5841876, essv5895866, essv5764206, essv5422317, essv5898705, essv6339584, essv6118260, essv5457970, essv5772007, essv5856125, essv5847654, essv6415426, essv5885132, essv5857406, essv6343307, essv6024990, essv6459311, essv6076478, essv5752178, essv5805728, essv5866246, essv6200649, essv6043936, essv6277016, essv6571582, essv5785895, essv5933689, essv6511508, essv6291488, essv6446883, essv6244475, essv6059727, essv6284470, essv5571539, essv6473565, essv5522234, essv6364029, essv5738588, essv6172042, essv5866232, essv5465939, essv6476638, essv5899740, essv6406904, essv5897477, essv5569049, essv5466525, essv6116496, essv6386986, essv6322513, essv5577244, essv6392066, essv5885036, essv5475842, essv6212950, essv6542588, essv5918426, essv5957716, essv5627360, essv6311764, essv6047629, essv6461729, essv5654302, essv6023287, essv6232723, essv6589052, essv6054389, essv5414072, essv5425434, essv5945477, essv6519532, essv5915299, essv6538556, essv5442274, essv6592545, essv5583120, essv6463512, essv6317385, essv6460297, essv5607930, essv5660077, essv5951683, essv5633618, essv5606822, essv5945650, essv5468825, essv6323226, essv5675499, essv6087775, essv6116997, essv6338432, essv6163232, essv6589071, essv6246157, essv6548919, essv5862343, essv5482572, essv6402974, essv5471258, essv5624868, essv5972414, essv6448306, essv5804900, essv5701628, essv5463587, essv6177129, essv6453940, essv6524903, essv6569365, essv6373973, essv5758316, essv5723223, essv5477338, essv6288484, essv5679290, essv6503987, essv6561753, essv5716928, essv5464464, essv6298078, essv5989242, essv5997845, essv5537646, essv5441137, essv6278105, essv6040212, essv6046939, essv5775828, essv6326995, essv5876638, essv5591428, essv5745454, essv5970353, essv5447795, essv5599176, essv5622915, essv5729466, essv6251626, essv5995755, essv5559672, essv6585004, essv6418952, essv6050675, essv6560331, essv5491654, essv5553188, essv5599515, essv5761698, essv5913595, essv6086933, essv5999537, essv6321789, essv5766048, essv5582209, essv5496164, essv6521451, essv5820146, essv6213017, essv6134160, essv6038912, essv6009849, essv5737295, essv6533333, essv6558186, essv6020164, essv5879167, essv5560961, essv5412287, essv5837727, essv6255231, essv6080191, essv5853230, essv5610464, essv6063958, essv6152625, essv6082648, essv6457226, essv5883612, essv6119727, essv5619915, essv5889673, essv5458575, essv6383273, essv5528431, essv6397193, essv5728703, essv5840863, essv5971514, essv6478242, essv6475151, essv5500269, essv5727090, essv5549023, essv5899371, essv5737532, essv5751914, essv6578159, essv5581217, essv6367482, essv6572858, essv5683759, essv6251257, essv6049318, essv5692789
SamplesHG01437, HG01061, HG00437, NA18562, NA19676, NA18620, NA19394, NA12383, HG01060, HG00542, HG01173, HG01356, HG00143, NA19703, NA19397, HG01462, HG00608, NA19909, HG00142, NA19664, HG00361, HG01359, HG00524, NA19399, NA19914, HG01052, HG00187, HG01079, HG01389, HG01374, HG01066, HG00151, NA20813, NA19359, HG00699, NA19355, NA19393, NA20332, NA19684, NA18606, HG00179, HG01051, NA20356, NA19920, HG01140, HG00693, HG00337, NA19374, NA19373, HG01350, NA19379, HG01366, HG01070, HG00501, NA19382, NA19728, HG01351, NA19448, HG00689, NA20586, NA18982, NA18635, NA20317, HG01492, HG00610, HG01354, NA19457, NA19313, HG01083, NA19138, HG01365, HG00334, NA20287, HG00185, NA20336, NA19904, HG00243, NA20291, NA19130, HG00158, NA19404, HG01134, HG00512, HG00281, HG00139, HG00277, HG01067, HG00236, NA18868, HG01072, NA19372, NA19371, NA19385, NA19471, HG01440, HG00182, NA20811, NA19901, NA19725, NA18520, HG00159, HG01048, HG01133, NA19445, HG00253, NA19451, HG00464, HG00108, NA18614, HG01353, HG00137, HG01136, NA19908, NA19657, NA19437, HG01187, HG01171, HG00282, NA19707, NA18934, HG00328, HG00428, NA19462, NA20809, HG00653, HG01095, HG00657, HG01515, NA19455, NA19663, HG00533, NA18871, HG00619, HG00708, NA18548, HG00740, HG01047, HG00284, HG01073, HG00273, HG00373, HG00479, HG00331, HG01101, HG00525, NA19452, HG00463, NA19469, NA19318, NA19395, NA12546, HG01107, HG01075, NA19436, NA18576, NA18546, NA19685, HG01148, NA19375, HG00258, HG00254, HG00265, NA18559, NA19712, NA19434, NA19747, HG00353, HG00580, HG00375, HG01551, HG00136, HG00638, NA19444, HG00278, NA19380, NA19010, HG01357, HG01174, HG01375, HG00237, NA19439, NA19428, NA19324, NA19311, HG01137, HG00319, HG01108, NA19360, NA06986, HG00339, HG00125, NA20341, NA19818, NA19376, HG00614, HG00111, HG01491, HG00312, NA19438, HG00342, HG00267, HG01055, NA20510, NA20289, HG00310, HG00186, HG00112, HG00698, NA19213, HG00252, HG01377, NA18989, NA19312, HG01125, NA20322, NA19463, NA18623
Known GenesZNF484
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671782
Frequency
Sample Size1151
Observed Gain0
Observed Loss217
Observed Complex0
Frequencyn/a


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