A curated catalogue of human genomic structural variation

Variant Details

Variant: esv2665192

Internal ID9584611
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89901367..89902730hg38UCSC Ensembl
chr16:89967775..89969138hg19UCSC Ensembl
Allele length
AssemblyAllele length
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
AnalysisNo reference, merging analysis
Pubmed ID23128226
Accession Number(s)esv2665192
Sample Size1151
Observed Gain0
Observed Loss128
Observed Complex0

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