A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665192



Internal ID9584611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89901367..89902730hg38UCSC Ensembl
chr16:89967775..89969138hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg381364
hg191364
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5560972, essv6581508, essv6163309, essv6172346, essv5976704, essv6391905, essv6237872, essv6347124, essv6399654, essv6170762, essv6553283, essv5616026, essv6211840, essv6432190, essv5733986, essv6429804, essv6070811, essv5554355, essv6185616, essv5748997, essv5501854, essv5492070, essv6456073, essv5942978, essv6376233, essv5508181, essv6037415, essv6029513, essv5535021, essv5942484, essv5731798, essv5757318, essv5615371, essv6539045, essv5435502, essv5887077, essv5480374, essv6254168, essv6529818, essv5913647, essv6592608, essv6445474, essv6272957, essv5486867, essv6531462, essv5822633, essv6378652, essv5506514, essv5600096, essv6495014, essv6485296, essv6331761, essv6226112, essv5505966, essv6015808, essv5849491, essv6073585, essv6098361, essv5442519, essv5549413, essv5681090, essv5770819, essv6269753, essv6041105, essv6266415, essv5888355, essv6440450, essv5686556, essv6356329, essv5997831, essv6441325, essv6104856, essv5630155, essv6162611, essv6090282, essv6283788, essv5489926, essv6558083, essv6236451, essv5472976, essv6447619, essv5598130, essv5470521, essv6184608, essv6541244, essv5742708, essv6078494, essv6470698, essv6170584, essv5705454, essv6020381, essv6008461, essv5994947, essv5545656, essv6230556, essv6348630, essv6271142, essv5928512, essv6265847, essv5821118, essv5575755, essv5734787, essv5499292, essv6420824, essv5900336, essv5844004, essv6451608, essv5848973, essv6557558, essv5401585, essv6238456, essv6323092, essv6095960, essv5493845, essv6423442, essv6185001, essv6144134, essv6085684, essv5729573, essv6018923, essv6115715, essv6070511, essv5949369, essv6316077, essv6081381, essv6146744, essv6205111, essv6547351
SamplesHG00323, HG00613, NA12718, HG00152, HG00607, NA18616, NA20771, NA11930, HG00619, NA18534, HG00344, NA18530, NA18535, HG01052, HG00705, HG00437, HG00500, HG01173, NA18612, NA20796, NA18526, HG00449, NA18570, NA19003, HG00463, HG00614, HG00577, HG00428, HG00475, HG00148, NA20786, HG00553, HG00139, NA18541, HG00683, HG00698, HG00651, HG00699, NA18950, HG00479, NA18596, NA18632, HG00244, HG00543, HG00154, NA19062, HG00321, HG00556, NA18627, NA19059, NA19076, HG00421, HG00583, NA20811, NA18622, NA18960, HG01048, NA18990, HG00689, NA18636, NA18592, NA07048, NA18547, NA12400, NA18637, HG00174, NA18982, HG00254, HG00276, HG00237, HG00662, NA20769, HG00436, HG00620, HG00653, NA18572, HG00629, HG00559, NA19657, HG00560, HG00265, HG00672, NA20814, NA19909, NA18613, HG00513, HG00524, NA20582, HG00512, HG00534, HG00525, NA19074, HG00377, NA19789, HG00589, NA18606, HG00120, NA18940, NA12890, NA18582, HG00427, NA18597, HG00590, NA18599, HG00663, HG00262, NA18560, NA18544, HG00608, NA18577, HG00654, HG00656, HG00422, NA18610, NA19070, NA18984, HG00690, HG00473, HG00684, NA20502, NA19087, HG00702, HG00704, HG00278, HG00136, NA12775, NA19058, HG00531
Known GenesTCF25
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665192
Frequency
Sample Size1151
Observed Gain0
Observed Loss128
Observed Complex0
Frequencyn/a


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