A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672184



Internal ID9938289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:59148389..59148723hg38UCSC Ensembl
chr20:57723444..57723778hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5428071, essv6379065, essv6197400, essv5768716, essv6173964, essv6078760, essv6115857, essv5522891, essv5470802, essv5619401, essv5941679, essv6359485, essv6221203, essv5398978, essv5726855, essv6489461, essv5472245, essv5894611, essv5750609, essv6482412, essv5545216, essv6055275, essv5670808, essv5538222, essv5968222, essv6377863, essv5924465, essv6587709, essv6543310, essv6231486, essv6295886, essv6170332, essv5507082, essv5486216, essv6094082, essv6445856, essv6074702, essv6368057, essv5916502, essv5898002, essv6330083, essv5512658, essv5533626, essv6416001, essv6154250, essv5828431, essv5953407, essv5826970, essv6231507, essv6570881, essv5804088, essv5723479, essv5457278, essv5697164, essv5424804, essv6450353, essv6002314, essv5617835, essv5607682, essv5559457, essv5566956, essv6327682, essv5845578, essv6435498, essv5931557, essv5872860, essv6580340, essv5683366, essv6456398, essv6397209, essv5792360, essv6382113, essv6586507, essv6433860, essv5440825, essv5783843, essv5606165, essv5398438, essv6418342, essv6011789, essv6447713, essv5702217, essv5645893, essv6254768, essv6379007, essv6366647, essv5462803, essv6568260, essv6551570, essv5743357, essv6338242, essv5954819, essv6476756, essv5399655, essv5604379, essv6267863, essv6465714, essv6553788, essv6555874, essv6545902, essv5510587, essv6051587, essv5786356, essv6031213, essv5480536, essv5641549, essv6410548, essv5418951, essv6252138, essv5848690, essv5922620, essv6482600, essv6341807, essv5878404, essv5706569, essv6068141, essv5879134, essv6525331, essv5935372, essv5699604, essv5507265, essv6475688, essv6184009, essv5694491, essv5931698, essv5922088, essv6240111, essv5925747, essv5900614, essv6144955, essv5503764, essv6078986, essv5481196, essv6538748, essv6067199, essv6578855, essv6246543, essv5758204, essv5442465, essv5616732, essv5466626, essv5424278, essv5764330, essv6059458, essv5661800, essv5966065, essv6516599, essv6263634, essv5546262, essv6530706, essv6587185, essv6501336, essv6070459, essv6397679, essv6392705, essv5643762, essv6366461, essv6050662, essv6583619, essv6491902, essv5952616, essv5890691, essv6036228, essv5918654, essv5480627, essv6331101, essv5797909, essv5878762, essv5656827, essv5543292, essv6343409, essv6018667, essv6124321, essv6285548, essv6143153, essv6449891, essv6187950, essv5432748, essv5633499, essv5696752, essv6161750, essv6395519, essv5853182, essv5965694
SamplesNA19394, NA12383, NA12717, NA19648, HG01173, HG01356, NA19397, NA18924, NA18947, NA11829, NA19204, NA18861, HG01052, NA19332, NA18980, NA20531, HG00315, HG00306, NA20532, HG00367, HG00318, NA18504, NA20332, NA18959, NA19190, NA19098, NA20806, HG00271, NA12813, NA20814, NA19446, NA19374, NA19373, NA18519, NA19201, NA18489, NA20589, HG01488, NA12891, NA20769, NA18942, HG00736, NA20768, NA19457, NA19313, HG00334, NA19384, HG00158, NA20541, NA12761, HG01134, NA20759, NA20539, NA19383, HG00335, HG00106, NA12156, HG00236, NA18868, NA19137, NA11932, NA12044, NA19207, NA19172, NA19317, HG01440, NA19159, HG00309, NA19901, NA18520, NA19239, HG01048, NA20342, NA12828, NA18975, HG00323, NA19985, NA18867, NA20515, NA19451, HG00264, HG00108, HG01124, HG00260, HG00313, NA20535, NA19908, NA19247, NA19210, NA20800, NA19437, HG00176, HG00282, NA12003, NA19152, HG00190, NA18956, NA19391, NA19455, HG00344, NA18871, NA18976, HG00239, NA18981, HG01390, HG00324, HG00273, NA19655, HG00373, NA11893, NA18856, NA18912, NA12892, HG00117, NA18853, HG01334, NA19452, NA12144, NA20828, NA18523, NA19160, NA12778, NA18858, HG01107, NA19436, NA18974, NA20765, NA12043, NA18953, HG01148, NA19401, NA19375, HG00124, HG00254, NA19108, NA19147, HG00375, HG00136, NA19435, NA19240, HG00278, NA20520, NA19144, NA19428, NA19311, NA20544, HG00116, HG00125, NA20341, NA19398, NA19328, NA18501, NA06994, NA18971, HG00312, NA19438, NA20582, NA19472, NA19223, HG00329, HG00342, NA19713, NA19093, HG00310, NA19102, HG00280, HG00131, NA19116, NA20826, NA18972, HG00252, NA19129, NA18488, HG01082, HG00171, NA20322, NA18968, NA18511, NA20585, NA18487, HG01437, NA19153, NA20509, NA19676
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672184
Frequency
Sample Size1151
Observed Gain0
Observed Loss184
Observed Complex0
Frequencyn/a


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