A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641604



Internal ID6681689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:3635328..3636918hg38UCSC Ensembl
Innerchr18:3635338..3636909hg38UCSC Ensembl
Outerchr18:3635319..3636928hg38UCSC Ensembl
chr18:3635327..3636917hg19UCSC Ensembl
Innerchr18:3635337..3636908hg19UCSC Ensembl
Outerchr18:3635318..3636927hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg381591
hg191591
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15779759, essv15779791, essv15779671, essv15779799, essv15779694, essv15779780, essv15779806, essv15779726, essv15779670, essv15779846, essv15779823, essv15779863, essv15779859, essv15779685, essv15779808, essv15779714, essv15779851, essv15779682, essv15779733, essv15779745, essv15779748, essv15779734, essv15779789, essv15779673, essv15779686, essv15779725, essv15779858, essv15779690, essv15779737, essv15779706, essv15779753, essv15779770, essv15779832, essv15779819, essv15779677, essv15779736, essv15779795, essv15779703, essv15779810, essv15779793, essv15779860, essv15779683, essv15779724, essv15779701, essv15779744, essv15779802, essv15779830, essv15779768, essv15779718, essv15779794, essv15779847, essv15779867, essv15779811, essv15779684, essv15779787, essv15779838, essv15779870, essv15779840, essv15779695, essv15779711, essv15779834, essv15779715, essv15779850, essv15779678, essv15779796, essv15779786, essv15779861, essv15779765, essv15779857, essv15779746, essv15779839, essv15779837, essv15779848, essv15779705, essv15779797, essv15779669, essv15779679, essv15779836, essv15779841, essv15779783, essv15779804, essv15779803, essv15779845, essv15779680, essv15779790, essv15779675, essv15779807, essv15779749, essv15779798, essv15779800, essv15779816, essv15779699, essv15779707, essv15779719, essv15779785, essv15779833, essv15779865, essv15779672, essv15779773, essv15779817, essv15779723, essv15779828, essv15779697, essv15779727, essv15779743, essv15779827, essv15779855, essv15779822, essv15779767, essv15779728, essv15779750, essv15779821, essv15779856, essv15779731, essv15779869, essv15779809, essv15779687, essv15779747, essv15779709, essv15779868, essv15779778, essv15779777, essv15779815, essv15779843, essv15779689, essv15779698, essv15779854, essv15779755, essv15779700, essv15779871, essv15779751, essv15779676, essv15779824, essv15779668, essv15779688, essv15779766, essv15779842, essv15779763, essv15779814, essv15779782, essv15779826, essv15779720, essv15779844, essv15779779, essv15779754, essv15779722, essv15779738, essv15779752, essv15779732, essv15779691, essv15779772, essv15779825, essv15779820, essv15779740, essv15779693, essv15779696, essv15779716, essv15779758, essv15779764, essv15779774, essv15779674, essv15779710, essv15779760, essv15779735, essv15779812, essv15779702, essv15779708, essv15779788, essv15779756, essv15779829, essv15779853, essv15779784, essv15779741, essv15779792, essv15779742, essv15779864, essv15779849, essv15779866, essv15779862, essv15779692, essv15779704, essv15779717, essv15779761, essv15779801, essv15779681, essv15779813, essv15779721, essv15779730, essv15779771, essv15779769, essv15779712, essv15779835, essv15779739, essv15779805, essv15779762, essv15779831, essv15779713, essv15779775, essv15779776, essv15779729, essv15779757, essv15779781, essv15779852, essv15779818
SamplesHG02879, HG03684, NA20281, NA18621, HG00881, HG01813, HG01926, HG02250, HG02291, HG01440, NA18616, HG02275, NA18951, HG02138, NA20809, NA18534, HG02025, HG02164, NA18952, HG00705, HG02086, HG01342, NA20510, NA19310, HG00565, HG00736, HG00632, HG01800, HG01794, HG02513, NA19072, HG03295, NA19455, HG01845, HG02152, NA18603, NA18993, NA18948, HG02260, HG01085, NA19334, NA19331, NA18969, NA18972, HG02722, NA19010, HG02002, HG02884, NA18542, HG02105, HG02379, HG02314, HG00683, HG02389, HG01958, NA18994, HG02322, HG02274, NA18965, HG03380, NA19355, HG01871, HG01936, HG01841, NA18950, HG02047, HG01812, HG02982, HG02082, HG02402, HG02312, HG04238, HG02155, HG03575, NA18992, HG01392, HG00406, HG02121, NA18622, NA18960, HG01595, HG02032, NA18990, HG00689, HG02373, HG03770, NA18531, NA18592, NA19083, HG01815, NA19440, HG01556, NA18976, NA19256, NA19075, HG00451, HG00634, HG00982, NA18634, NA18643, HG00237, HG01596, HG01599, HG00662, NA18539, HG00867, HG01797, HG03063, NA19213, HG01437, HG02131, NA19785, NA18747, NA18645, NA19189, NA19759, NA19372, NA18954, HG04161, NA19024, HG00560, HG02573, NA18558, HG02017, NA19901, NA18748, NA18942, NA18961, HG02087, HG00513, HG01260, HG02384, NA21100, HG02364, HG02072, HG02536, NA19091, HG03713, HG01531, HG02180, HG02299, HG02190, NA18543, HG03028, NA18619, HG00445, NA19729, NA18907, NA19723, HG00611, HG00650, HG02154, NA18740, HG01953, HG02351, HG03045, NA18565, HG03267, HG03702, HG01862, HG02035, NA18560, NA18989, HG00118, HG03815, HG02561, NA18614, HG01802, NA19770, HG01464, NA19225, HG00656, HG02678, NA19732, HG00422, NA19006, HG01808, HG01855, HG02271, HG00623, HG02353, HG00625, HG01842, HG02136, NA18574, HG01374, HG00473, HG01631, NA19087, NA19200, NA19385, HG01976, HG04182, HG01863, HG02396, NA18519, HG03824, HG02367, HG00531, HG02512, HG02179, NA18553, HG04107, NA19439
Known GenesDLGAP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641604
Frequency
Sample Size2504
Observed Gain0
Observed Loss204
Observed Complex0
Frequencyn/a


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