A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2422149



Internal ID8252597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:122582018..122592081hg38UCSC Ensembl
Innerchr10:124341534..124351597hg19UCSC Ensembl
Innerchr10:124331524..124341587hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3810064
hg1910064
hg1810064
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5077696, essv5075905, essv5003833, essv5150983, essv5012785, essv5084338, essv5046581, essv5083842, essv5050775, essv5156596, essv5045031, essv5126353, essv5125503, essv5093094, essv5028093, essv5040612, essv5011527, essv5065378, essv5011348, essv5104652, essv5130168, essv5086943, essv5129996, essv5131456, essv5082705, essv5067608, essv5031407, essv5002847, essv5093536, essv5106939, essv5089135, essv5045450, essv5049518, essv5012225, essv5070734, essv5124383, essv5046134, essv5149723, essv5118590, essv5099118, essv5155302, essv5151467, essv5136674, essv5047698, essv5148909, essv5055202, essv5117512, essv5056717, essv5042602, essv5122121, essv5102268, essv5067038, essv5120823, essv5115496, essv5080712, essv5041962, essv5046116, essv5035035, essv5019393, essv5147168, essv5121821, essv5080235, essv5027060, essv5087724, essv5069917, essv5058109, essv5104932, essv5030731, essv5015840, essv5142497, essv5085927, essv5026430, essv5003971, essv5067896, essv5103727, essv5097226, essv5041145, essv5129483, essv5082538, essv5094868, essv5092238, essv5057236, essv5112088, essv5025200, essv5127601, essv5009089, essv5106539, essv5036551, essv5159884, essv5081705, essv5099093, essv5076255, essv5149843, essv5114518, essv5104432, essv5145134, essv5116454, essv5156322, essv5135761, essv5077701, essv5127481, essv5128766, essv5046087, essv5109969, essv5053488, essv5043610, essv5002865, essv5122932, essv5089401, essv5048286, essv5036053, essv5095438, essv5049420, essv5108562, essv5148214, essv5149541, essv5083773, essv5127082, essv5116292, essv5102645, essv5074278, essv5051654, essv5101069, essv5146579, essv5016076, essv5023929, essv5008871, essv5057912, essv5045913, essv5117152, essv5017856, essv5146477, essv5088092, essv5152730, essv5029981, essv5025465, essv5088303, essv5004164, essv5054222, essv5133932, essv5057801, essv5086213, essv5047331, essv5132981, essv5118561, essv5079287, essv5007699, essv5115608, essv5135705, essv5089926, essv5132588, essv5091788, essv5005890
SamplesNA18623, NA21440, NA19065, NA18740, NA19074, NA20898, NA18577, NA19676, NA10865, NA12739, NA20588, NA19394, NA18998, NA12383, NA21097, NA18157, NA17969, NA21111, NA20543, NA21423, NA19794, NA20877, NA20508, NA12843, NA12344, NA20873, NA18603, NA21723, NA21717, NA18124, NA21408, NA18616, NA20517, NA11891, NA18526, NA12400, NA18633, NA20771, NA12399, NA20894, NA18627, NA20846, NA17986, NA20861, NA18995, NA18595, NA12802, NA20900, NA18619, NA20769, NA18105, NA18942, NA20768, NA18161, NA19138, NA19079, NA20910, NA19760, NA18611, NA12761, NA12275, NA21611, NA21109, NA12156, NA20812, NA21454, NA19677, NA18112, NA10850, NA18131, NA12815, NA20889, NA20884, NA19796, NA18557, NA21442, NA21417, NA18640, NA20755, NA18150, NA18638, NA12748, NA20854, NA18951, NA18605, NA17976, NA21313, NA20535, NA18747, NA12760, NA12752, NA18674, NA10863, NA18109, NA18956, NA18694, NA20760, NA19663, NA20875, NA18976, NA18948, NA19097, NA21438, NA10838, NA18981, NA18566, NA21441, NA17979, NA19774, NA21086, NA20859, NA21112, NA11894, NA12056, NA20856, NA12264, NA19059, NA19009, NA18555, NA06985, NA19160, NA20542, NA20534, NA19436, NA18953, NA18978, NA21117, NA18952, NA21144, NA18564, NA20909, NA19144, NA21123, NA20792, NA21390, NA19311, NA17970, NA18643, NA18943, NA21094, NA12347, NA06986, NA18594, NA18631, NA07435, NA20582, NA21102, NA18609, NA17987, NA18149, NA20502, NA21490, NA18955
Known GenesDMBT1
MethodSNP array
AnalysisTo assess copy number variation we merged and analysed the probe level intensity data from both the Affymetrix and Illumina arrays.
PlatformNot specified
Comments
ReferenceAltshuler_et_al_2010
Pubmed ID20811451
Accession Number(s)esv2422149
Frequency
Sample Size1184
Observed Gain0
Observed Loss153
Observed Complex0
Frequencyn/a


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