A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672413



Internal ID9591832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89732697..89732883hg38UCSC Ensembl
chr16:89799105..89799291hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38187
hg19187
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5536384, essv5566147, essv5831104, essv5895112, essv5806096, essv6221789, essv5739921, essv5969090, essv6429182, essv6413443, essv6327331, essv6564052, essv5831451, essv6101706, essv6583216, essv5698798, essv6229856, essv6411507, essv6515154, essv6412057, essv5476147, essv5979596, essv6175933, essv5427515, essv5651180, essv6584720, essv6346584, essv6028054, essv6008227, essv6126376, essv5619360, essv5840469, essv6158981, essv6104432, essv5715526, essv5630166, essv5843909, essv5835719, essv6264297, essv6520306, essv6124453, essv6420961, essv5487329, essv5821008, essv6463029, essv6227504, essv5838390, essv6583049, essv5586368, essv6513383, essv6009286, essv6012004, essv6487738, essv5501692, essv6132890, essv6264737, essv6361908, essv6024843, essv6173851, essv5725013, essv5982798, essv5728769, essv5806473, essv5935986, essv6301599, essv5711950, essv5515443, essv6165385, essv5884578, essv6053004, essv6551530, essv5902138, essv6102804, essv6201040, essv6460692, essv5927915, essv6013293, essv6353440, essv5586142, essv5477565, essv5604114, essv5835118, essv5687068, essv5446603, essv6369455, essv5400861, essv6385445, essv6025501, essv6521976, essv5666561, essv5855493, essv5627182, essv6352947, essv5581921, essv6340477, essv6319548, essv6515397, essv6350325, essv6106649, essv6115953, essv5424703, essv6399483, essv5574219, essv5593750, essv5670327, essv6087358, essv5417746, essv5423622, essv5806165, essv6288991, essv6480186, essv5580463, essv5656602, essv6264374, essv5525784, essv6579746, essv5428356, essv5560407, essv6236758, essv5964206, essv5985305, essv5566304, essv6141328, essv5636810, essv5781018, essv6301762, essv6516634, essv5577376, essv6219635, essv5540469, essv5875077, essv6100112, essv5979834, essv6123327, essv6442064, essv6418500, essv5567418, essv5732124, essv5908794, essv6492521, essv5567245, essv6120035, essv6273413, essv6552028, essv6565634, essv5824450, essv6005548, essv5473632, essv5811110, essv6477065, essv5549821, essv5441298, essv6413798, essv5776239, essv6011404, essv5615995, essv5788705, essv6427458, essv6528954, essv5721343, essv6428081, essv5472071, essv6392331, essv5609424, essv6108897, essv5821665, essv6015876, essv5562826, essv6189383, essv5676726, essv6083731, essv6189416, essv6434728
SamplesHG00323, HG01357, HG00613, NA11881, HG00309, HG01515, NA12154, HG00252, HG00318, NA07347, HG00257, NA07037, NA20522, HG00619, NA18534, HG00344, NA18530, NA18535, HG01072, HG01052, NA19819, HG00437, NA20516, HG00500, HG01173, HG01083, NA18612, HG00112, NA20796, NA18526, HG00449, HG00310, NA19003, HG00261, NA18545, NA18603, HG00463, HG00614, HG00475, HG00148, NA19920, NA20778, HG00553, HG00139, HG00683, HG00698, NA19834, HG00111, HG00404, HG00651, HG00280, HG00366, HG00699, NA20755, NA18943, HG01171, HG00353, HG00479, NA18596, NA20340, HG00269, NA18632, HG00543, HG00154, HG01107, HG00321, HG00556, NA20505, NA19076, HG00140, NA18622, HG00180, HG01048, HG01061, HG00231, NA18990, HG01047, HG00689, NA18636, NA18592, HG00628, NA12761, NA11894, NA12400, NA18637, NA20336, HG00174, HG00254, HG00276, HG00237, NA12144, NA20341, HG00662, NA20769, HG00436, HG00620, HG00108, HG00653, NA18572, HG01066, NA19375, HG00325, HG00263, NA12275, NA20334, HG00260, HG00501, HG00672, HG00282, HG01170, HG01356, HG00249, HG00103, NA18613, HG00513, HG00524, NA20582, HG00512, HG00534, HG00525, NA19789, HG00236, HG00589, NA18940, NA18582, NA20525, NA18597, HG00590, NA18552, HG01095, NA18599, HG00611, NA20799, NA20518, HG00663, NA12156, NA18560, NA18544, NA19818, NA18577, HG00654, HG01390, NA20513, NA12399, HG00656, HG00422, NA18610, NA19070, NA20792, NA18611, HG00324, HG00690, NA20528, NA18549, HG00473, HG01462, NA20524, HG00684, NA19758, HG00336, HG00476, NA20502, HG00671, NA19087, HG00345, HG00702, HG00704, NA19385, NA19750, HG00278, HG00136, HG00531, HG01067
Known GenesZNF276
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672413
Frequency
Sample Size1151
Observed Gain0
Observed Loss173
Observed Complex0
Frequencyn/a


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