A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599951



Internal ID6640213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:24964838..24965516hg38UCSC Ensembl
Innerchr4:24964839..24965516hg38UCSC Ensembl
Outerchr4:24964838..24965517hg38UCSC Ensembl
chr4:24966460..24967138hg19UCSC Ensembl
Innerchr4:24966461..24967138hg19UCSC Ensembl
Outerchr4:24966460..24967139hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38679
hg19679
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11370784, essv11370881, essv11370719, essv11370737, essv11370746, essv11370818, essv11370706, essv11370697, essv11370860, essv11370722, essv11370771, essv11370720, essv11370798, essv11370911, essv11370864, essv11370822, essv11370792, essv11370877, essv11370858, essv11370750, essv11370884, essv11370903, essv11370780, essv11370900, essv11370887, essv11370909, essv11370904, essv11370738, essv11370865, essv11370687, essv11370811, essv11370821, essv11370851, essv11370862, essv11370749, essv11370832, essv11370801, essv11370883, essv11370896, essv11370729, essv11370837, essv11370777, essv11370897, essv11370714, essv11370854, essv11370761, essv11370763, essv11370788, essv11370683, essv11370727, essv11370828, essv11370754, essv11370776, essv11370764, essv11370724, essv11370835, essv11370870, essv11370682, essv11370739, essv11370695, essv11370895, essv11370759, essv11370876, essv11370805, essv11370779, essv11370817, essv11370826, essv11370807, essv11370840, essv11370794, essv11370889, essv11370797, essv11370716, essv11370744, essv11370789, essv11370735, essv11370731, essv11370774, essv11370866, essv11370747, essv11370907, essv11370766, essv11370905, essv11370901, essv11370741, essv11370688, essv11370713, essv11370736, essv11370748, essv11370892, essv11370898, essv11370745, essv11370910, essv11370841, essv11370769, essv11370678, essv11370855, essv11370823, essv11370850, essv11370810, essv11370799, essv11370701, essv11370691, essv11370711, essv11370913, essv11370899, essv11370733, essv11370868, essv11370712, essv11370804, essv11370873, essv11370768, essv11370694, essv11370912, essv11370891, essv11370808, essv11370785, essv11370844, essv11370906, essv11370908, essv11370856, essv11370882, essv11370698, essv11370880, essv11370710, essv11370879, essv11370791, essv11370803, essv11370732, essv11370693, essv11370707, essv11370783, essv11370787, essv11370709, essv11370793, essv11370847, essv11370760, essv11370806, essv11370743, essv11370836, essv11370752, essv11370781, essv11370703, essv11370679, essv11370702, essv11370755, essv11370765, essv11370770, essv11370708, essv11370734, essv11370705, essv11370813, essv11370871, essv11370725, essv11370888, essv11370838, essv11370869, essv11370816, essv11370690, essv11370849, essv11370861, essv11370848, essv11370829, essv11370825, essv11370726, essv11370875, essv11370819, essv11370902, essv11370830, essv11370814, essv11370839, essv11370728, essv11370834, essv11370689, essv11370772, essv11370686, essv11370827, essv11370845, essv11370684, essv11370824, essv11370857, essv11370874, essv11370681, essv11370753, essv11370859, essv11370680, essv11370740, essv11370786, essv11370699, essv11370756, essv11370820, essv11370852, essv11370872, essv11370894, essv11370767, essv11370718, essv11370717, essv11370692, essv11370730, essv11370878, essv11370833, essv11370796, essv11370790, essv11370809, essv11370802, essv11370843, essv11370723, essv11370700, essv11370758, essv11370775, essv11370842, essv11370886, essv11370704, essv11370831, essv11370757, essv11370846, essv11370867, essv11370685, essv11370762, essv11370863, essv11370800, essv11370778, essv11370696, essv11370715, essv11370721, essv11370815, essv11370812, essv11370751, essv11370795, essv11370782, essv11370885, essv11370890, essv11370893, essv11370742, essv11370773, essv11370853
SamplesHG01878, HG02580, NA19137, NA19207, HG02317, NA19248, HG02427, HG03121, NA19625, HG02882, HG03567, HG01241, NA18520, HG02621, NA20890, HG02398, NA19089, NA20859, HG03280, HG03784, NA19222, HG00956, NA18933, HG01988, HG03084, HG01089, HG02023, HG02546, NA20906, HG01859, HG03856, NA19209, NA19093, HG01858, HG03066, HG03129, HG01885, HG00449, HG03196, HG02255, HG00707, HG03295, NA19223, NA19455, HG02450, HG02943, NA18877, HG02153, HG04026, HG02104, HG03894, HG00428, HG02722, NA18947, HG01491, HG01524, NA18608, NA18865, HG02508, HG01286, HG02977, HG02146, HG02694, NA18507, HG02676, HG02660, HG03103, HG02277, HG01571, HG03229, HG01990, HG04100, HG03199, HG01860, HG02778, HG03808, HG03039, NA19308, HG02047, HG02133, HG02973, NA18868, HG01812, NA19043, HG02870, NA19117, HG02836, NA19028, HG02081, HG03088, HG00556, HG02390, NA19428, NA20856, HG01363, NA19239, NA19314, HG02634, NA19323, HG04188, HG00593, HG00583, HG03300, HG02716, NA18622, NA19197, NA19443, HG00759, NA20908, HG03578, HG01572, HG02012, HG03442, HG03717, NA18991, HG00689, HG00628, HG01795, HG02557, HG03241, NA19351, HG02016, HG03464, HG01556, NA19774, HG03100, HG03539, NA18973, NA18916, HG04063, NA18593, NA20892, HG00407, HG02756, HG00662, NA19324, NA19190, NA19213, HG02392, HG03773, NA19377, HG02151, HG03126, NA19759, HG02449, HG01413, NA19372, HG02382, HG00653, NA19374, NA19375, HG02285, HG02562, HG01806, NA19027, NA19102, HG00559, HG02922, NA18522, HG03547, HG01853, NA18941, HG01369, NA19901, HG03514, HG03974, HG01356, HG01923, HG01139, HG03518, HG02771, HG03800, NA18878, NA19909, HG00513, HG02384, NA19707, HG01805, HG01341, HG01894, NA19091, NA19307, NA19789, HG02085, HG03132, HG01566, HG02301, NA19729, HG03303, HG03888, HG02819, NA18599, HG02923, HG01973, NA20332, HG02134, NA19431, HG02035, HG03172, NA20298, HG02628, HG02481, NA19446, HG01390, HG02079, NA19740, NA19770, HG02489, NA19225, HG03074, NA18917, HG02678, HG03258, NA18499, NA18571, HG02476, HG03270, HG02286, NA19095, HG03449, HG02485, HG02136, NA18532, NA18853, HG02798, HG03515, HG00684, NA19185, NA19454, HG01869, HG01890, HG02064, NA18881, HG01976, HG03095, HG02839
Known GenesCCDC149
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599951
Frequency
Sample Size2504
Observed Gain0
Observed Loss236
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer