A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv786e199



Internal ID20124088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:41277355..41279252hg38UCSC Ensembl
chr20:39905995..39907892hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg381898
hg191898
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2675927, esv2666382
SamplesHG00613, HG01441, NA19012, NA18621, NA19312, NA12489, HG00537, HG01440, NA18595, NA18616, NA18951, NA18534, HG01353, NA19081, NA19819, NA19437, HG00705, HG00437, HG00500, HG01083, NA18501, HG00131, HG00565, NA19311, HG00160, HG01079, NA19319, NA19359, HG01365, NA19334, HG00189, HG00577, NA19453, HG00428, HG00475, NA18947, HG00542, NA18573, HG00139, NA19144, HG00122, NA19210, NA19379, HG00698, HG01188, HG00581, NA18963, NA19685, HG00404, HG00651, NA19004, NA19678, HG00280, HG00557, HG01134, NA19682, HG00366, HG00578, HG00146, NA18965, NA19472, NA19467, HG01551, NA18873, NA18950, HG01171, NA18868, NA20340, HG00269, HG00554, HG00256, NA19077, HG01107, NA19062, HG00321, HG01550, NA19463, NA19914, HG01148, HG00242, NA11919, NA18912, NA19982, NA19085, HG00346, HG01140, NA18967, HG00593, HG00472, HG01375, NA19390, HG00421, HG00583, NA12004, HG01378, NA18635, NA19057, NA19068, NA19660, NA19675, HG00140, NA12155, HG00180, NA18618, NA19443, NA18623, NA19471, NA20757, NA19444, HG00610, NA18990, HG00372, HG00692, HG01183, HG01047, NA18636, NA19396, HG01124, NA18592, NA19083, HG00628, NA20127, NA18638, NA18956, NA19398, HG00338, HG00178, HG00125, HG01360, HG01113, HG01136, HG01253, HG00634, HG00243, NA19679, HG00284, NA19700, NA12144, NA19082, HG00584, NA19316, NA20341, NA18539, NA12751, HG01497, NA19000, NA19213, HG00159, HG00267, NA19377, HG01437, NA19395, NA19080, NA18537, NA18620, HG01465, NA19372, NA18633, HG00653, HG01191, NA19703, NA19375, NA19393, NA20760, NA19373, NA19384, HG00629, NA18986, NA19238, NA19005, NA19119, NA19098, HG00239, NA18941, NA19664, HG00501, HG01069, NA19704, HG00478, NA18961, HG00277, NA19347, NA19332, HG00740, HG00524, HG00512, HG00534, NA19707, NA20766, NA18562, NA19074, HG01060, HG01383, NA19711, NA18985, HG00589, NA19777, NA18940, HG00151, NA18619, NA18987, NA10851, NA18999, HG00427, NA18597, HG00595, NA19376, HG01095, NA18983, HG00443, NA18599, NA19391, HG00611, NA12749, NA06984, NA18867, NA19403, NA18565, HG00138, NA12156, NA18631, NA19431, NA18989, HG00580, NA19747, NA18544, NA19434, NA18602, NA19818, NA19099, NA19446, HG00654, HG00530, NA19064, NA18944, NA19063, NA19327, NA12399, NA19717, HG00656, NA12546, NA19655, HG00142, HG01366, NA18499, NA18924, HG00708, HG01108, NA20758, NA19240, NA19346, HG00275, HG00324, HG00625, HG00690, NA18532, NA18574, HG00183, HG00442, HG01374, HG00473, NA18981, NA19350, HG00137, HG00626, HG00684, HG01377, NA18615, HG00143, NA19448, NA20538, HG00702, NA19200, NA19385, HG00278, NA19661, NA19779, NA12775, NA19058, NA19466, HG00531, HG01354, NA19439, HG00312, HG00327, HG00361, NA18964, NA12718, NA19445, NA19625, HG00152, HG01518, NA19436, HG00318, HG00536, HG00607, NA07037, HG01072, NA20785, HG01052, NA18975, NA07056, HG01342, HG00369, HG00449, HG00310, NA18550, HG00261, NA12340, NA20802, NA18948, NA19430, NA19451, NA18972
Known GenesZHX3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv786e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss314
Observed Complex0
Frequencyn/a


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