A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633700



Internal ID7020507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20889644..20953797hg38UCSC Ensembl
Innerchr14:20889644..20953797hg38UCSC Ensembl
Outerchr14:20889437..20953965hg38UCSC Ensembl
chr14:21357803..21421956hg19UCSC Ensembl
Innerchr14:21357803..21421956hg19UCSC Ensembl
Outerchr14:21357596..21422124hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3864154
hg1964154
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv381e214
Supporting Variantsessv14925899, essv14925805, essv14925850, essv14925808, essv14925799, essv14925836, essv14925800, essv14925795, essv14925843, essv14925882, essv14925837, essv14925814, essv14925793, essv14925826, essv14925901, essv14925822, essv14925818, essv14925889, essv14925897, essv14925902, essv14925880, essv14925849, essv14925859, essv14925876, essv14925854, essv14925811, essv14925860, essv14925865, essv14925813, essv14925894, essv14925835, essv14925796, essv14925845, essv14925798, essv14925861, essv14925895, essv14925877, essv14925885, essv14925892, essv14925810, essv14925815, essv14925868, essv14925833, essv14925852, essv14925873, essv14925832, essv14925839, essv14925879, essv14925797, essv14925831, essv14925816, essv14925869, essv14925874, essv14925896, essv14925840, essv14925801, essv14925794, essv14925846, essv14925886, essv14925841, essv14925807, essv14925855, essv14925809, essv14925824, essv14925844, essv14925871, essv14925806, essv14925827, essv14925802, essv14925870, essv14925872, essv14925866, essv14925881, essv14925834, essv14925825, essv14925821, essv14925857, essv14925803, essv14925875, essv14925812, essv14925898, essv14925804, essv14925847, essv14925838, essv14925842, essv14925888, essv14925830, essv14925853, essv14925856, essv14925817, essv14925891, essv14925864, essv14925819, essv14925900, essv14925828, essv14925867, essv14925863, essv14925884, essv14925890, essv14925851, essv14925887, essv14925893, essv14925829, essv14925848, essv14925862, essv14925823, essv14925820, essv14925883, essv14925878, essv14925858
SamplesHG02890, HG02944, HG03378, HG02583, HG02272, NA19466, HG03548, HG03163, HG03175, NA18881, HG02419, NA18917, NA18486, HG02323, HG03297, HG03139, HG02734, HG03577, HG03372, NA18510, NA19374, HG03133, HG02621, NA18489, HG03452, HG02952, HG02383, NA20756, HG03370, HG03040, HG01242, HG02281, NA19923, HG02703, NA20278, NA18874, HG01628, NA19917, NA19137, HG03212, NA19172, HG02588, NA19036, HG03744, HG03380, HG02427, NA19456, NA19025, HG03055, NA20127, NA20318, HG02479, HG02570, NA19247, NA18934, HG02334, HG02582, NA18933, NA19984, HG03291, NA19455, NA19043, HG01088, HG02307, HG02976, NA18907, HG03311, HG03123, HG01392, HG03472, HG02429, HG03136, HG02283, NA19099, HG03391, NA19318, NA19395, HG02675, HG01990, HG02484, HG01896, HG02722, HG03567, NA18608, NA19401, NA19440, HG02667, NA19108, NA19019, HG02308, NA19473, HG02721, HG01958, NA19144, HG02314, NA19835, HG02971, HG03442, NA19468, HG03063, HG03410, NA19116, NA19711, HG02681, HG02851, HG02284, HG03198, HG02808, NA19429, HG03271
Known GenesECRP, RNASE3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633700
Frequency
Sample Size2504
Observed Gain0
Observed Loss110
Observed Complex0
Frequencyn/a


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