A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665740



Internal ID9585160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:180639155..180639304hg38UCSC Ensembl
chr5:180066155..180066304hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6442465, essv5885610, essv6370530, essv6012190, essv6159937, essv6476290, essv6541709, essv6292048, essv6409417, essv5562197, essv5899118, essv6290381, essv5406704, essv6263517, essv6037933, essv6002263, essv6391858, essv6447630, essv5755022, essv6194092, essv5545191, essv6057630, essv5410286, essv6367896, essv5417958, essv6466998, essv6313971, essv5591945, essv5422615, essv6294579, essv5584746, essv6266052, essv6269156, essv6414202, essv6014738, essv5440580, essv6498698, essv5630256, essv6583094, essv6290136, essv5914779, essv6549486, essv5873272, essv6088341, essv6194054, essv6314588, essv6062334, essv5782703, essv5471799, essv5419376, essv5504918, essv6587075, essv5887791, essv6193237, essv5568079, essv6409276, essv6523655, essv5528747, essv5608398, essv6218765, essv6386491, essv6189257, essv5705103, essv6190038, essv6194022, essv6450492, essv6077673, essv5903402, essv5493025, essv5733539, essv6319559, essv5889441, essv5912382, essv5723351, essv6396132, essv5469359, essv5986232, essv6515019, essv5582560, essv5641452, essv5835250, essv5881108, essv6331068, essv5584090, essv6079956, essv6532036, essv5613783, essv5998578, essv6529100, essv6277749, essv5782604, essv5675210, essv6239260, essv5930954, essv5991241, essv5930350, essv6058447, essv5625556, essv5948445, essv6438360, essv6485223, essv5768802, essv6028299, essv5417461, essv5540862, essv5820618, essv6411320, essv5567848, essv5978318, essv6364329, essv5962015, essv5738411, essv5610267, essv5853920, essv5811509, essv6451283, essv6036250, essv6152689, essv6426478, essv6208556, essv5460318, essv5537299, essv5633935, essv6065826, essv5614743, essv5776497, essv5554269, essv6453536, essv6357140, essv5489807, essv5629953, essv5641265, essv6498199, essv6279956, essv5875802, essv5852839, essv6100019, essv6293947, essv6383215, essv6479187, essv5499112, essv6174741, essv6499067, essv5690110, essv6119984, essv5717714, essv6523652, essv6121037, essv6465945, essv6353773, essv5739173, essv6145988, essv6020294, essv6440539, essv6445147, essv6397878, essv5832561, essv5604346, essv5688134, essv5910796, essv5789351, essv5682126, essv5506623, essv5540902, essv5576129, essv6416326, essv6534185, essv5861655, essv6273480, essv6018826, essv6587684, essv5939730, essv6213705, essv6167760, essv6177379, essv5995651, essv6245682, essv5698608, essv6250304, essv5575248, essv5558438, essv5705678, essv6506087, essv6057519, essv5578691, essv6046342, essv5836060, essv6154009, essv6530064, essv5890275, essv6013346, essv6430222, essv6548812, essv6488610, essv6208382, essv6289875, essv6580871, essv5644587, essv6166363, essv6258172, essv5816718, essv5527247, essv5855437, essv5938039, essv6052244, essv6171544
SamplesHG00323, HG00613, NA12827, NA18621, HG00313, HG00252, HG00536, HG00607, HG01440, HG00257, HG00619, NA18534, HG00344, NA18530, HG00418, HG01072, HG01052, NA18561, NA19404, HG00328, HG00705, HG00437, HG00500, HG01173, HG01083, NA18612, HG00464, HG00310, NA18550, HG00261, NA18545, HG01389, HG00463, HG00657, HG00614, HG01051, HG01365, HG01492, HG01082, HG00428, HG00475, HG00375, HG01174, HG00326, NA18573, HG01350, HG00139, NA19379, HG00701, HG00683, HG00698, HG01188, HG00111, HG00334, HG00581, HG00651, HG00280, HG00335, HG00557, HG01101, HG00331, HG00319, HG00253, HG00699, NA18557, HG00353, HG00479, HG00256, NA18632, HG00342, HG00543, HG00154, HG01107, NA18559, HG00339, HG00556, NA19428, HG00346, NA18624, HG00250, HG01375, HG00421, HG00583, HG00337, NA18635, NA18536, HG00140, NA18576, NA18622, HG00259, NA18623, HG01061, HG00692, HG01183, HG00689, NA18636, HG00330, NA18638, HG00338, HG00533, HG00419, HG00125, NA12829, NA18637, NA18593, HG00254, HG00276, HG00284, HG00237, HG00343, HG00584, HG00662, HG00436, NA19360, HG00620, HG01437, HG00108, NA18537, NA18620, NA18633, HG00653, NA19374, HG00268, HG01066, HG00325, HG00263, HG00260, HG01073, HG00501, HG00672, HG00282, HG01170, HG00232, HG01069, HG00249, HG00478, HG00277, HG01351, NA18613, HG00513, HG00524, HG00329, HG00512, HG00534, HG01070, HG00525, NA18562, HG01060, NA18579, HG00589, NA18606, NA18543, NA18940, NA18582, HG00427, NA18597, HG00590, NA19138, HG00443, HG01334, HG00650, NA19403, HG00663, HG00580, NA18544, HG00448, NA18602, HG00608, NA18577, HG00654, HG01390, HG00281, HG00285, NA18499, HG00422, NA19371, HG00708, HG01108, NA18610, HG00693, HG00251, HG00320, HG00275, HG00324, HG00690, NA18532, NA18549, NA18853, HG00442, HG01374, HG00473, HG00137, HG00684, HG00336, HG00476, NA20502, HG00671, HG00702, HG00704, HG00271, HG00278, HG00136, NA19746, HG00531, HG01067, HG00327
Known GenesFLT4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665740
Frequency
Sample Size1151
Observed Gain0
Observed Loss206
Observed Complex0
Frequencyn/a


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