A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656892



Internal ID9576311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:98238007..98238826hg38UCSC Ensembl
chr9:101000289..101001108hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38820
hg19820
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5604652, essv6371662, essv5617328, essv5517097, essv6416519, essv6111763, essv6182961, essv6269573, essv5525592, essv5893170, essv5938655, essv6041053, essv6399064, essv6486503, essv5716956, essv6476167, essv5498531, essv5842624, essv5481082, essv5969319, essv5863217, essv6475907, essv5554192, essv6276056, essv5866627, essv5483658, essv5695203, essv5743064, essv6243287, essv5715952, essv5788431, essv5996614, essv5421347, essv6099913, essv6316937, essv6538950, essv5443066, essv5818715, essv6186071, essv5470779, essv6350682, essv6417792, essv6240226, essv6311800, essv6052949, essv6582205, essv5748789, essv5858495, essv6582951, essv5462771, essv5627687, essv6256265, essv6461176, essv5654043, essv6147258, essv6424887, essv6548169, essv5666459, essv5943632, essv5438910, essv5469643, essv6096225, essv5403207, essv5551840, essv5690462, essv6519552, essv5877126, essv5949767, essv6343906, essv6322796, essv6484599, essv6167909, essv6148690, essv6034715, essv5753490, essv5972710, essv6558812, essv5539601, essv5828279, essv6534242, essv5546628, essv5446386, essv6489817, essv6393775, essv5460736, essv6420120, essv5593929, essv5694116, essv6381274, essv6324799, essv6441802, essv5537379, essv5536611, essv5587052, essv5836362, essv6049583, essv5962200, essv5963145, essv6444020, essv5505809, essv6090252, essv5678328, essv5835132, essv6285338, essv6306448, essv5690202, essv5728709, essv6230530, essv5534231, essv6172529, essv6324660, essv5403511, essv6017022, essv5751152, essv5405476, essv6162230, essv6495933, essv6591490, essv5404795, essv6552633, essv5433984, essv5826480, essv5825323, essv5680472, essv6398604, essv5964333, essv6334828, essv6569745, essv5462287, essv6413000, essv6266881, essv6353708, essv6276816, essv6084543, essv6443332, essv5639324, essv6064295, essv6445968, essv5912203, essv5967392, essv6152258, essv5620569, essv6293280, essv5500345, essv6265750, essv5964222, essv6393671, essv5847811, essv6008133, essv6002770, essv6107521, essv6522590, essv5998167, essv5901718, essv5946055, essv6124347, essv6390378, essv5411921, essv5927116, essv6444877, essv5902489, essv5429317, essv5965354, essv5536077, essv5921167, essv5721998, essv6499526, essv5997904, essv6163394, essv5406939, essv5717720, essv6511227, essv6217692, essv5986930, essv5760342, essv6555777, essv6586522, essv5470379, essv5751993, essv5807487, essv6421588, essv5991556, essv5525735, essv5416364, essv6055590, essv6246707, essv6574949, essv5715812, essv6568014, essv5733941, essv6067550, essv6334173, essv5637320, essv6023510, essv5918133, essv6475250, essv5681077, essv6022723, essv5428623, essv5552872, essv6511162, essv5602594, essv5730460, essv5818530, essv5839107, essv6309172, essv5825842, essv5909242, essv6021269, essv5795835, essv6524539, essv5759767, essv6059584, essv5829687, essv5900267
SamplesHG00323, NA20281, NA19137, NA19207, NA18870, NA19248, NA19152, NA19445, NA19625, NA18861, NA19436, NA20787, NA19712, NA18520, NA07037, NA19321, NA20278, NA18871, HG01052, NA19819, NA18933, NA18523, NA19114, NA18874, HG01342, NA19209, NA18501, NA19093, NA19401, NA20796, NA19469, HG00261, NA18511, NA19223, NA06989, NA19435, NA20294, NA20296, NA20775, NA19430, NA20759, NA18516, NA19317, NA19359, NA19334, NA19331, NA19453, NA19451, NA20816, NA18517, NA19338, NA20342, NA19920, NA18489, NA19461, NA19144, NA12058, NA18507, HG01204, HG00280, NA19257, HG00177, NA19701, NA19236, NA19355, NA20322, NA18505, NA19472, NA18873, NA19147, HG00188, HG01171, NA19438, NA18868, NA20340, NA20770, NA20532, NA19463, NA19914, NA19428, NA18912, NA19383, NA18934, HG00179, HG01140, NA20356, HG01375, NA19390, NA19068, NA19917, NA20811, HG00180, NA19197, NA19443, NA19471, NA19107, NA19444, HG00231, NA20783, NA19396, NA18856, HG00628, NA19397, NA20127, NA19398, NA19440, NA19908, NA19985, NA19256, NA19835, NA20336, NA18916, HG00174, NA19457, NA19316, NA20341, NA19190, NA19213, NA19247, NA19360, NA19313, NA19377, NA19380, NA19395, NA19153, NA19129, NA19172, NA19189, NA19372, NA20291, HG01191, NA19375, NA20126, NA20348, NA20512, NA19373, NA19384, NA18498, NA18923, NA18486, NA18522, NA18510, NA20344, NA18502, NA19713, NA19098, NA19901, NA18504, NA19704, HG00249, NA18487, NA18858, NA19347, HG01080, NA19332, NA19909, NA18613, NA20582, NA19707, NA20766, NA19131, NA19328, NA18910, NA19382, NA19318, NA19711, NA19462, NA19235, NA19921, NA12272, NA18909, NA19391, NA20276, NA20332, NA18867, NA19394, NA19116, NA20289, NA20287, NA19434, NA19818, HG00608, NA19099, NA19446, NA20317, NA19770, NA20810, NA19225, NA18917, NA19160, HG00142, NA18924, NA19371, NA19198, NA19916, HG01108, NA19470, NA20792, NA19130, NA19346, HG00641, NA19204, HG01374, NA19350, NA18908, NA19381, HG00143, NA19448, NA19468, NA19200, NA18519, NA19466, NA19746, HG01354, NA19439
Known GenesTBC1D2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656892
Frequency
Sample Size1151
Observed Gain0
Observed Loss215
Observed Complex0
Frequencyn/a


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