A curated catalogue of human genomic structural variation

Variant Details

Variant: dgv786e199

Internal ID20124088
Location Information
TypeCoordinatesAssemblyOther Links
chr20:41277355..41279252hg38UCSC Ensembl
chr20:39905995..39907892hg19UCSC Ensembl
Allele length
AssemblyAllele length
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
AnalysisNo reference, merging analysis
Pubmed ID23128226
Accession Number(s)dgv786e199
Sample Size1151
Observed Gain0
Observed Loss314
Observed Complex0

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