A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668206



Internal ID2901293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:27826528..27826814hg38UCSC Ensembl
chr8:27684045..27684331hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg38287
hg19287
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6183208, essv5974864, essv6109794, essv6582948, essv6353116, essv6127066, essv6525218, essv5495660, essv6391989, essv6592143, essv5470314, essv6595077, essv6441020, essv5828727, essv5958503, essv6445317, essv6127703, essv6426984, essv5432859, essv5624197, essv6164407, essv5622212, essv6164962, essv5973491, essv5906535, essv6012102, essv5505767, essv5948403, essv5609220, essv6185054, essv5558306, essv5413491, essv5897153, essv5530373, essv5961442, essv5440312, essv6350797, essv5836165, essv6332131, essv6042738, essv5558219, essv6366259, essv5630146, essv5911802, essv6281811, essv6111665, essv6307241, essv6146147, essv5875333, essv5572359, essv6190746, essv6570465, essv5476032, essv5439237, essv6080917, essv5584257, essv6339444, essv5473455, essv5930852, essv6416984, essv5914879, essv6360124, essv5962215, essv5857151, essv5655619, essv5763635, essv5806225, essv6233070, essv5793359, essv6325383, essv5860817, essv6171223, essv6584026, essv6202575, essv6108219, essv5613222, essv6196458, essv5850557, essv5577165, essv5532560, essv5543269, essv5803252, essv5935409, essv6490203, essv5803181, essv6315809, essv5553294, essv5657949, essv5774870, essv6226407, essv5468914, essv5516838, essv5656686, essv6457175, essv5891107, essv5679934, essv6053465, essv6339802, essv5716495, essv6227413, essv5612499, essv6222922, essv6231099, essv5633662, essv6245061, essv5667232, essv6597834, essv6410518, essv5454401, essv5445321, essv6569342, essv6434945, essv5800144, essv5564823, essv5647378, essv6238907, essv5906376, essv6037169, essv5566964, essv6528051, essv6057740, essv5463998, essv5490668, essv6388737, essv5901277, essv6509747, essv5689789, essv5555415, essv6506539, essv6193857, essv5925476, essv6223990, essv5432660, essv6419571, essv6116262, essv6234948, essv6511631, essv5894405, essv5439223, essv6178059, essv5558367, essv6095124, essv5883903, essv6361848, essv6497804, essv5608018, essv5893450, essv6194116, essv6231997, essv6077126, essv5779654, essv6413394, essv6205597, essv6153180, essv5443890, essv6040860, essv5414479, essv5504796, essv5861726, essv6204593, essv5654602, essv6483081, essv5472634, essv6070605, essv6584659, essv5931223, essv5754600, essv6216813, essv5677261, essv6358861, essv5754500, essv5446255, essv6364644, essv5790138, essv6424775, essv6192621, essv5434403, essv6048796, essv5794142, essv5754337, essv5766823, essv6400669, essv6487516, essv6589273, essv6250284, essv6023836, essv5887469, essv6375527, essv6157298, essv6494674, essv5610514, essv5621914, essv5409976, essv6428235, essv5564964, essv5630903, essv6127656, essv6513589, essv6394684, essv6093092, essv6050916, essv6582795, essv5577520, essv5740614, essv5612661, essv5843016, essv5931301, essv5981574, essv6513259, essv5718022, essv6351109, essv5580323, essv5824190, essv6017744, essv5595247, essv6309089, essv5886279, essv6560611, essv5747766, essv5430756, essv5649194, essv6411706, essv6291080, essv5472514, essv5957309, essv6227785
SamplesHG00613, NA19137, NA19207, NA19152, HG00734, NA18861, NA18605, HG00607, NA12748, NA18520, NA18595, NA11930, NA18951, NA20527, NA20278, NA18534, NA18530, HG00418, HG01052, NA19819, NA18523, NA20752, NA18975, HG00705, HG00437, HG00500, HG01173, NA18612, NA19209, NA19401, HG00449, NA11918, NA18570, NA19072, HG00707, HG01079, NA18948, HG00463, NA18516, HG00614, HG01365, NA12813, NA19334, HG01082, NA18972, NA18517, HG00475, NA18947, NA18608, HG00148, NA20778, NA20786, NA18542, NA19144, NA19210, HG00683, NA19834, HG01188, HG00651, HG00557, HG01101, NA19108, NA19701, NA18488, HG00737, NA18505, NA19147, HG00353, HG00479, NA19654, NA18632, HG00342, HG00543, HG00154, NA18559, HG00321, HG00556, NA11919, NA12763, NA12843, HG01384, NA18967, NA19054, NA19076, NA20819, HG00472, NA19390, HG00421, NA12004, NA18635, NA19917, HG00140, NA18576, NA18623, HG00692, HG01183, HG00689, NA18636, NA18856, HG00628, NA19397, NA18638, NA19440, NA19066, HG00338, HG00533, HG00419, NA18547, NA18976, NA20282, NA18916, NA19056, HG00276, HG00284, HG01187, NA19700, HG00237, HG00343, NA19082, HG00662, NA12751, NA19000, HG00159, HG00620, NA19380, HG01437, NA19395, NA19153, NA12046, NA18537, NA18633, HG00653, NA19374, NA19703, NA18498, NA18486, NA18968, NA06986, NA19238, NA18510, NA18502, NA19119, HG01073, NA18558, NA19098, HG00501, HG00232, NA19704, HG00478, NA18564, NA18858, NA18942, NA18961, HG01080, NA18613, HG00513, HG00524, HG00512, NA19707, HG00246, NA19131, NA19159, NA18910, NA18579, NA18974, NA18985, HG00589, NA18945, NA18606, NA18940, NA18597, HG00590, NA18552, HG01095, HG00443, NA18599, NA18907, NA19391, NA19201, HG00611, HG00650, NA19394, NA19403, NA18565, HG00663, NA19116, NA18989, NA18971, NA19818, HG00608, NA19452, NA20507, HG00530, NA11992, HG00285, NA19399, HG00656, NA19160, NA18499, NA18571, HG00422, NA19371, NA20543, NA18610, HG01125, NA11829, NA19171, NA19240, HG01498, HG00690, NA20528, NA18549, NA19204, HG00442, HG00473, NA18981, NA20524, HG01377, NA06994, HG00671, HG00702, NA19200, NA20519, NA07000, HG00531, HG00327
Known GenesPBK
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668206
Frequency
Sample Size1151
Observed Gain0
Observed Loss226
Observed Complex0
Frequencyn/a


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