A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3587526



Internal ID6627828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151360740..151441151hg38UCSC Ensembl
chr1:151333216..151413627hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3880412
hg1980412
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10145315, essv10145292, essv10145329, essv10145360, essv10145398, essv10145331, essv10145399, essv10145279, essv10145380, essv10145441, essv10145277, essv10145425, essv10145474, essv10145290, essv10145390, essv10145302, essv10145311, essv10145374, essv10145464, essv10145456, essv10145442, essv10145333, essv10145412, essv10145304, essv10145340, essv10145382, essv10145361, essv10145385, essv10145282, essv10145416, essv10145293, essv10145347, essv10145323, essv10145431, essv10145371, essv10145428, essv10145285, essv10145284, essv10145430, essv10145479, essv10145336, essv10145419, essv10145369, essv10145319, essv10145483, essv10145422, essv10145309, essv10145359, essv10145386, essv10145414, essv10145468, essv10145291, essv10145448, essv10145278, essv10145322, essv10145388, essv10145469, essv10145415, essv10145365, essv10145367, essv10145362, essv10145432, essv10145458, essv10145350, essv10145397, essv10145418, essv10145434, essv10145429, essv10145410, essv10145407, essv10145389, essv10145384, essv10145453, essv10145296, essv10145433, essv10145405, essv10145341, essv10145345, essv10145274, essv10145394, essv10145452, essv10145376, essv10145281, essv10145316, essv10145377, essv10145337, essv10145461, essv10145383, essv10145306, essv10145321, essv10145310, essv10145342, essv10145487, essv10145317, essv10145326, essv10145334, essv10145381, essv10145451, essv10145473, essv10145307, essv10145298, essv10145455, essv10145471, essv10145472, essv10145391, essv10145447, essv10145435, essv10145280, essv10145312, essv10145335, essv10145462, essv10145299, essv10145373, essv10145457, essv10145330, essv10145402, essv10145476, essv10145438, essv10145364, essv10145286, essv10145338, essv10145339, essv10145437, essv10145409, essv10145443, essv10145366, essv10145486, essv10145387, essv10145395, essv10145294, essv10145460, essv10145300, essv10145482, essv10145401, essv10145421, essv10145446, essv10145450, essv10145288, essv10145406, essv10145478, essv10145283, essv10145351, essv10145352, essv10145370, essv10145378, essv10145445, essv10145272, essv10145379, essv10145357, essv10145481, essv10145344, essv10145439, essv10145289, essv10145459, essv10145301, essv10145449, essv10145275, essv10145470, essv10145295, essv10145475, essv10145426, essv10145320, essv10145403, essv10145276, essv10145466, essv10145318, essv10145313, essv10145404, essv10145424, essv10145392, essv10145440, essv10145349, essv10145454, essv10145467, essv10145375, essv10145354, essv10145413, essv10145396, essv10145305, essv10145297, essv10145328, essv10145427, essv10145436, essv10145287, essv10145400, essv10145477, essv10145408, essv10145314, essv10145363, essv10145465, essv10145324, essv10145417, essv10145353, essv10145355, essv10145372, essv10145444, essv10145303, essv10145343, essv10145463, essv10145271, essv10145332, essv10145273, essv10145348, essv10145356, essv10145368, essv10145420, essv10145346, essv10145411, essv10145308, essv10145480, essv10145358, essv10145393, essv10145423, essv10145325, essv10145327, essv10145485, essv10145484
SamplesHG03684, HG02122, HG02724, HG02725, HG03697, HG03968, HG03858, NA19312, HG03963, HG03015, HG00356, HG02793, NA20874, HG01846, HG03760, HG03785, HG03861, HG02275, HG03668, HG02736, HG03784, HG01852, HG03479, HG03977, HG01918, HG01089, HG03744, HG03886, HG04202, HG02546, HG03703, HG02655, HG01859, HG03478, HG03868, HG03874, HG02549, HG02601, HG02734, HG02792, HG04096, HG04211, NA19435, HG01777, HG03643, HG02648, HG01197, HG03896, HG01325, HG01850, HG02783, HG03663, HG02681, HG04026, HG04229, HG03653, HG03973, HG03234, NA19461, HG03680, NA20805, HG02790, HG03019, HG03491, HG03967, HG03229, HG04200, HG01961, HG03960, HG04020, HG02685, HG04100, HG02789, HG01871, HG02150, HG03949, HG04023, HG02778, HG03947, HG01968, HG03687, HG03897, HG01917, HG03667, HG02455, HG03955, HG04238, HG04098, HG02775, HG04210, HG02699, HG03235, HG03736, HG03672, HG02654, HG01392, HG01305, HG02009, HG03882, HG02121, HG03953, HG03686, HG01061, HG02577, HG03774, HG01088, HG03681, HG01620, HG03770, HG03862, HG03844, HG03965, HG03871, HG01977, HG04042, HG04063, HG03781, HG04227, HG03971, HG03848, HG03780, HG02603, HG03869, HG01242, HG01874, HG03731, HG03757, HG03773, HG02304, HG03786, HG04017, HG02127, HG02537, HG04025, HG03792, HG02102, HG01806, HG03660, HG03753, HG03754, HG02073, HG03782, HG02439, HG04080, HG04239, HG03849, HG01170, HG02558, HG01176, HG03740, HG03873, HG02787, HG02651, HG02780, HG03433, HG02545, HG04093, NA21095, HG02052, HG02072, HG03738, HG03978, HG03945, HG02690, HG03943, HG02345, HG04235, HG03691, HG03237, HG01095, HG01971, HG01973, HG04022, HG03745, HG03789, HG03790, HG01695, HG03679, HG03866, HG04019, HG01872, HG03238, HG03694, HG03986, HG03644, HG03771, HG03716, HG02953, HG01303, HG01893, HG03872, HG03018, HG02262, HG02079, HG03999, HG02252, HG04018, HG02687, HG03890, HG01323, HG03857, HG01855, HG03718, HG03016, HG03838, HG04015, HG04054, HG02555, HG03695, HG03720, NA20519, HG03490, HG03991, HG02774, HG03777, NA20339, HG03775
Known GenesPOGZ, PSMB4, SELENBP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3587526
Frequency
Sample Size2504
Observed Gain0
Observed Loss217
Observed Complex0
Frequencyn/a


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