A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677015



Internal ID9943120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:66585399..66586040hg38UCSC Ensembl
Outerchr15:66585242..66586193hg38UCSC Ensembl
Innerchr15:66877737..66878378hg19UCSC Ensembl
Outerchr15:66877580..66878531hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38952
hg19952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv456e199
Supporting Variantsessv6596688, essv5506380, essv5595481, essv5584772, essv5977503, essv5754141, essv6480413, essv5653687, essv5895463, essv6274278, essv6448455, essv6421284, essv5743356, essv5922138, essv5576305, essv5989100, essv6439298, essv5817036, essv5880317, essv5583592, essv5461343, essv6535600, essv5638678, essv5449485, essv5893741, essv5607223, essv6171462, essv6388958, essv6017712, essv5858233, essv5851003, essv5464529, essv6083421, essv6411992, essv6193565, essv6201439, essv6126682, essv5774002, essv6269531, essv5718463, essv6047024, essv5868017, essv5494411, essv5765699, essv5897525, essv5563710, essv5740092, essv5947145, essv6198304, essv5713842, essv5703795, essv5568191, essv5729604, essv5765713, essv6113384, essv6207506, essv5408905, essv5871052, essv6531112, essv6179744, essv6575357, essv6442275, essv5844700, essv5686058, essv5989294, essv6572043, essv6392682, essv6217225, essv5494128, essv5762548, essv5649066, essv6498492, essv5809151, essv6001395, essv6257616, essv6558955, essv5580444, essv6390865, essv6026582, essv5502837, essv6376107, essv5600405, essv6531896, essv6145035, essv5713966, essv6495649, essv6306797, essv6536708, essv6575994, essv5473143, essv6212669, essv6576310, essv6042237, essv6205647, essv5397700, essv6190869, essv6566830, essv5552924, essv6397550, essv6269302, essv6466423, essv5490751, essv5574959, essv6047212, essv6246143, essv5849880, essv6303290, essv6317338, essv6299050, essv6380408, essv6560361, essv5960281, essv6141778, essv6334664, essv5702731, essv6317616, essv5983677, essv6406409, essv6042546, essv6262723, essv5421806, essv5527920, essv6325436, essv5937703, essv5730798, essv6063196, essv6129189, essv5958619, essv5637472, essv6572067, essv6490223, essv6117912, essv6080864, essv6023229, essv5930380, essv6514656, essv5404403, essv5656014, essv6280128, essv6446550, essv6146610, essv5585332, essv5661244, essv5895534, essv6304650, essv5717508, essv5870942, essv6493722, essv6164612, essv6354381, essv6173757, essv6494663, essv6514564, essv6337952, essv6555660, essv6562510, essv5795810, essv6317481, essv6381372, essv6415880, essv6093686, essv6228364, essv6086351, essv5400381, essv5556792, essv5806878, essv6421723, essv6058454, essv5876811, essv5719253, essv6124429, essv6542957, essv6080646, essv6204380, essv5871108, essv6178981, essv5663256, essv5823715, essv6241787, essv6349366, essv5872213, essv5892175, essv5444509, essv6481079, essv5638822, essv6546268, essv5718053, essv5940356, essv5735868, essv5499043, essv5697126, essv6424347, essv5657005, essv6291482, essv6317967, essv5781488, essv5926770, essv5942071, essv5433526, essv5688530, essv5575045, essv6566559, essv5466766, essv5718040, essv6563798, essv5581679, essv5941407, essv6565895, essv6130366
SamplesNA20588, NA12383, HG01060, HG00189, NA11830, HG01173, NA19700, HG01098, NA12286, NA19914, HG00187, NA19332, HG01079, HG00100, NA11933, NA18599, HG01389, HG00315, NA20512, HG00318, NA12751, HG01465, NA12340, NA12058, NA20808, NA18616, NA20517, NA20507, NA19443, NA18870, NA12400, HG01051, HG00261, NA12413, NA12341, HG00337, NA20814, NA19068, HG00641, HG00138, NA19379, HG00589, HG00272, HG00501, NA20798, HG01351, NA20586, NA19723, NA20795, NA18547, NA19062, NA11992, HG00346, NA12283, HG01354, NA20540, NA19313, NA18571, NA12287, HG00369, NA20513, NA19681, NA18964, HG00537, HG00311, HG00243, HG00158, NA19404, NA12761, HG00512, HG00281, HG00139, NA12282, NA12275, HG01067, HG00335, HG00148, NA20775, HG01170, HG00236, NA11932, NA19172, NA19471, HG01440, HG00309, HG00182, HG00427, HG00160, HG00118, NA19725, HG01198, HG00159, HG01133, HG00178, NA18539, NA12748, HG01124, NA11831, HG00313, NA18605, HG00268, NA20524, HG01384, NA12003, HG01095, HG00657, HG00475, NA18516, NA19982, HG00320, HG00344, NA12718, NA20519, NA18910, NA20770, HG01073, NA18573, HG00273, HG00651, NA19449, NA19084, NA19655, HG00373, HG00479, NA20581, NA12829, NA11893, HG01197, NA18856, NA12249, HG00117, NA18853, NA12827, HG00276, HG00152, HG00146, NA12144, NA19469, HG00246, HG01204, HG01075, NA20765, NA12043, HG01148, HG00258, NA18632, NA19652, HG00254, HG00119, NA19390, NA18961, NA18543, NA19712, NA19434, NA12775, HG00366, NA19072, NA20804, NA19444, NA07051, NA19010, HG01357, NA20790, HG01375, NA19334, NA19470, NA20544, NA19786, NA19467, HG00116, NA07037, NA19783, HG00662, NA19085, NA18615, HG01342, NA12347, HG00339, HG00269, HG00125, NA19248, NA19779, NA12749, NA19716, HG01055, HG00174, HG00123, NA19102, NA18873, NA20807, NA19726, NA19080, HG00343, NA20528, HG00377, HG00372, HG01377, NA20502, HG00472, NA19129, HG01378, NA19755, HG01125, HG00345, NA12154, NA19074, NA18487, HG00553, HG00437
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677015
Frequency
Sample Size1151
Observed Gain0
Observed Loss209
Observed Complex0
Frequencyn/a


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