A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677815



Internal ID9943920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:112254556..112254900hg38UCSC Ensembl
Outerchr11:112254517..112254957hg38UCSC Ensembl
Innerchr11:112125279..112125623hg19UCSC Ensembl
Outerchr11:112125240..112125680hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg38441
hg19441
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6384853, essv5858847, essv5977019, essv5830367, essv6451571, essv6422888, essv6121651, essv5531376, essv6350726, essv6338431, essv5604152, essv5634073, essv6317976, essv6384256, essv5966471, essv6267264, essv6030598, essv6574301, essv5665667, essv5559335, essv5590547, essv6109385, essv6396083, essv5731332, essv6151157, essv5471603, essv6112372, essv6453112, essv5859298, essv6530390, essv5724042, essv6107695, essv5824454, essv5818896, essv5897037, essv5498094, essv6110249, essv6103596, essv5504425, essv5961635, essv5998322, essv6274612, essv5593384, essv6169745, essv5583448, essv6114059, essv5714967, essv6460394, essv5435194, essv5660106, essv5590897, essv6045646, essv6247034, essv6482438, essv6256193, essv6479121, essv6269340, essv5454473, essv5587931, essv5703477, essv5398900, essv6299619, essv5511375, essv6539042, essv5469747, essv5734253, essv6435579, essv5444725, essv5799827, essv6569818, essv5551075, essv5396354, essv6530527, essv6357726, essv5760057, essv6552183, essv5529188, essv6246708, essv6348907, essv6375483, essv6163802, essv6135736, essv6420450, essv5591215, essv6164881, essv5718279, essv6363214, essv5485414, essv5464561, essv5651615, essv6591647, essv5708132, essv6019752, essv5813519, essv6373319, essv6389889, essv5899588, essv5900131, essv5836318, essv6577844, essv5921237, essv5975821, essv6458630, essv5625790, essv5654462, essv5813465, essv5931023, essv6428204, essv5412619, essv6239610, essv5507080, essv6280939, essv6299573, essv6028793, essv5706621, essv6149774, essv5774676, essv5643046, essv5419184, essv5409892, essv6482623, essv6521742, essv6329139, essv6378970, essv5397800, essv5790911, essv5947075, essv5716291, essv5587932, essv5493683, essv5808681, essv6559451, essv5707806, essv6419814, essv5693674, essv5844875, essv5883940, essv6232700, essv6588886, essv5648796
SamplesNA12383, NA20761, HG00542, HG00442, NA11830, NA12842, NA19055, NA12286, NA19066, NA20783, NA18565, HG01079, NA12843, NA11920, NA20816, NA20813, NA20802, NA20805, NA18596, NA20808, HG01051, NA19920, NA20771, NA18510, NA20806, NA18602, NA20537, NA20796, NA18940, NA18550, NA18519, HG01366, NA18635, NA18567, NA20795, NA12348, NA19062, HG00334, NA20513, NA18964, NA20541, NA11930, HG00281, HG00139, NA20775, NA06984, NA20812, HG00262, NA11932, NA18560, NA11994, NA19075, NA19385, NA18986, NA19722, NA20811, HG00326, NA20757, NA20533, HG01124, NA20818, HG00543, HG00154, NA20800, NA18538, HG01171, NA19070, NA20505, NA20809, NA20521, HG00657, NA20810, NA20760, NA20536, NA19788, NA19658, NA18948, NA20770, HG00273, HG00651, HG00690, HG00479, NA20581, NA18499, NA12249, NA06989, HG00117, HG00525, HG00140, NA12827, NA18963, NA18570, NA12546, NA18541, NA20765, NA20799, NA20801, HG00119, NA18535, HG00285, NA18559, NA20815, NA19072, NA18950, HG00375, NA20520, NA19773, NA20790, NA19835, HG00237, HG00319, NA20516, NA20803, NA20797, NA07037, NA19085, NA12347, NA06986, NA19779, HG00342, NA19468, NA19474, HG00123, NA12830, NA20807, NA20758, NA20826, NA20528, NA18983, NA20503, NA18984, NA18989, NA18488, NA18624, NA12890, NA18623, NA19065, NA18612, NA18549, HG00437
Known GenesPLET1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677815
Frequency
Sample Size1151
Observed Gain0
Observed Loss140
Observed Complex0
Frequencyn/a


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