A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663511



Internal ID9929616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:125953623..125958529hg38UCSC Ensembl
Outerchr3:125953002..125959099hg38UCSC Ensembl
Innerchr3:125672466..125677372hg19UCSC Ensembl
Outerchr3:125671845..125677942hg19UCSC Ensembl
Cytoband3q21.2
Allele length
AssemblyAllele length
hg386098
hg196098
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6528830, essv5858634, essv6512818, essv5905028, essv6491159, essv6411594, essv5467033, essv6203677, essv5941491, essv5842790, essv5807930, essv6597718, essv5819982, essv6422752, essv5591528, essv5413595, essv6568755, essv6146429, essv5578864, essv5519932, essv5516119, essv5474190, essv5954200, essv5448523, essv6281461, essv5402618, essv6458454, essv5441288, essv5636148, essv6107685, essv5609126, essv6586675, essv5918252, essv5588641, essv6441057, essv5524269, essv5488635, essv6443617, essv6260406, essv6174930, essv6547430, essv6538616, essv6376005, essv6220368, essv5600624, essv6317441, essv6171540, essv6113687, essv5928724, essv6534827, essv6390083, essv6368306, essv5702919, essv5676810, essv5515745, essv5917303, essv5484335, essv6532786, essv6304854, essv6143566, essv5785749, essv5495797, essv6151413, essv6248005, essv6137116, essv5952653, essv5765480, essv6497782, essv5509545, essv5915459, essv6450983, essv5984852, essv5490727, essv6212221, essv5419847, essv6413321, essv5474030, essv6204335, essv6539502, essv6334842, essv6434849, essv6221097, essv5634154, essv6172071, essv5939436, essv6319478, essv5458749, essv6494797, essv5898477, essv5609578, essv6393278, essv5791699, essv5457268, essv5971545, essv5749750, essv5738999, essv6238228, essv6170822, essv6320012, essv6104744, essv6363009, essv6310023, essv6197745, essv6023782, essv5821199, essv5786393, essv5809731, essv5558499, essv6191075, essv6084879, essv5928520, essv5471760, essv6002336, essv6542034, essv6013334, essv6126258, essv6175538, essv5881774, essv5653122, essv6386613, essv6102319, essv6169135, essv6229213, essv5956993, essv6239783, essv5460046, essv5454519, essv6131893, essv5995932, essv6222706, essv5765639, essv5634378, essv6181658, essv5946983, essv6334211, essv5441325, essv6593671, essv5983943, essv6454334, essv6363680, essv5557635, essv5568574, essv5891204, essv6242743, essv6060617, essv6514019, essv5969147, essv5797573, essv5495031, essv5409189, essv5744221, essv5847594, essv5892809, essv5794413, essv6489820, essv6064870, essv5641689, essv5478683, essv5845530, essv5902503, essv5839438, essv5959533, essv5771047, essv6344369, essv5972413, essv5516184, essv6372961, essv5735980, essv6441869, essv5433769, essv6423440, essv5889772, essv6275153, essv6544258, essv6053268, essv5936466, essv6147851, essv5574169, essv6438466, essv6251433, essv6143198, essv6411878, essv6420466, essv6240728, essv6015167, essv5746947, essv6420443, essv6069697, essv5757636, essv5474417, essv6455635, essv5462825, essv5667873, essv5461490, essv5704385, essv6347766, essv6125627, essv6355164, essv5596057, essv6071614, essv5835209
SamplesNA19394, NA18502, HG01060, NA19701, HG01356, NA19703, NA19397, NA18924, HG01462, NA19909, NA19466, NA18508, HG01359, NA19704, HG01188, HG01389, HG01374, HG01066, NA19359, NA18486, HG01465, NA20294, NA19355, NA19393, NA19377, NA20346, HG01461, NA19443, NA19190, HG01051, NA19920, NA18510, NA19107, NA19446, NA19374, HG00641, NA19396, NA19381, NA19373, NA19171, NA19379, NA18519, NA19319, NA19382, NA19315, NA18489, HG01351, NA19448, HG01167, NA19119, NA18923, NA19198, NA20317, NA18916, NA19197, NA19457, NA19313, HG01083, NA19138, NA18498, NA20287, NA20336, NA19904, NA20291, NA19404, NA19383, HG01170, NA18868, HG01072, NA19372, NA19371, NA19235, NA19385, NA19172, NA19471, NA19317, NA19901, HG01198, HG00637, HG01048, NA20342, NA19456, NA19445, NA20127, NA18908, NA19985, NA18867, NA19451, HG01124, HG01183, HG01136, NA19908, HG00731, NA19437, HG01171, NA18934, NA19462, NA19347, NA19152, NA18933, HG00732, HG01095, NA19391, NA19327, NA19455, NA18516, NA19982, NA18910, NA18871, NA20344, NA18907, NA19461, NA19449, HG01197, NA18499, NA18856, NA19453, NA18912, HG01101, NA18853, NA19099, NA19257, NA19452, NA19225, NA18523, NA19318, NA18858, HG01204, NA19436, NA20296, NA19375, NA19440, NA18909, HG01190, NA19834, NA19321, NA19256, NA18517, NA20276, NA19434, NA19473, HG01551, HG01253, NA19435, HG00638, NA19444, NA19331, NA19380, HG01174, NA19334, HG01494, NA19439, NA19470, NA19428, NA19324, NA19311, HG01113, NA19467, HG01137, NA19360, HG01342, NA20341, NA19818, NA19376, NA19398, NA19328, NA18501, NA20348, NA19248, NA19438, NA19472, NA19223, NA20334, NA19468, NA19713, HG01055, NA19093, NA19102, NA18873, NA19711, NA19213, NA19900, HG01251, NA19430, NA18505, NA19129, NA19316, HG01125, NA20322, NA19463, NA18511, NA18522, HG01112, HG01097, HG01191, NA19429, NA19346, NA18487, HG01437, NA19153, NA19431
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663511
Frequency
Sample Size1151
Observed Gain0
Observed Loss201
Observed Complex0
Frequencyn/a


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