A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1189e199



Internal ID20124491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:28534679..28535564hg38UCSC Ensembl
chr7:28574297..28575182hg19UCSC Ensembl
Cytoband7p15.1
Allele length
AssemblyAllele length
hg38886
hg19886
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2668808, esv2673635, esv2673786, esv2659026
SamplesHG00613, HG01441, NA19012, NA19312, HG00157, NA12154, HG00252, HG01440, NA18520, NA18616, NA20771, NA19904, NA19819, NA20752, HG01173, HG01083, NA20510, HG00112, HG00464, NA20544, NA20796, NA19469, HG00261, NA19223, HG01098, NA06989, NA19435, NA20299, NA20296, HG00463, HG01051, HG01365, HG00117, NA20808, NA19453, HG01082, NA20816, HG01488, NA20529, NA18947, NA19449, NA20342, HG00173, HG00326, NA18573, HG00148, NA19920, NA20778, NA20786, HG00139, NA19461, HG00190, NA19379, HG00106, HG01167, NA19834, HG01188, NA20805, HG00111, HG00334, HG01204, NA12776, NA07051, HG00651, NA19004, HG00335, HG01101, HG01134, HG01168, NA19701, NA20798, NA12341, NA19472, NA19761, HG01171, NA20340, HG00247, HG00554, NA20770, HG00342, HG00115, HG00154, HG01107, NA19062, NA19463, HG00158, HG01148, NA19067, NA19428, NA20585, HG00242, NA11919, HG00346, NA18934, HG01140, HG01456, NA20356, NA20515, HG01375, NA19390, NA18566, HG00337, HG01378, NA11994, NA19068, NA19660, HG00638, NA18576, HG00259, HG00096, NA18623, NA19471, NA19900, NA20757, HG01048, NA19444, HG01061, NA18617, HG00372, HG01183, NA18991, NA18636, NA19396, NA18856, NA19397, NA20127, NA07048, NA12761, NA19440, HG00150, HG00258, NA11843, NA11831, NA12829, HG01136, NA20282, HG01253, NA19658, HG00243, NA19679, HG00276, HG00284, NA12777, NA19700, NA20341, HG00133, NA19324, NA20773, HG00114, NA19213, NA19676, NA19360, HG00159, HG00267, NA19380, NA19786, HG00124, NA12046, HG00108, NA12716, HG01465, NA19189, HG00233, NA20291, NA19703, HG00268, HG01066, NA19375, HG00732, NA19373, HG00325, NA12348, NA18923, NA20826, NA06986, NA20334, NA20344, NA19713, NA19731, NA19664, NA19901, HG01069, HG00249, NA11892, NA18487, HG00116, NA19347, NA20774, HG00103, NA19909, NA20797, NA20582, HG00153, HG00329, HG00512, HG00534, NA19707, HG00246, HG00525, NA12283, NA19074, HG01060, HG01383, NA20813, HG00236, NA19462, HG01149, NA19777, HG00120, NA19235, NA10851, HG01137, HG01190, NA19376, NA12272, HG00443, NA18909, NA19391, NA19078, HG00611, NA18867, NA19403, NA12413, NA12156, NA19116, HG00262, NA18631, NA19431, NA18560, HG01112, NA19719, NA18602, NA19818, NA19099, HG01390, NA19452, NA20507, NA20317, NA11830, HG00123, NA18917, NA19655, HG01366, NA18571, NA19916, NA20758, NA19470, HG00367, NA18984, NA11932, HG00566, HG01125, NA11829, HG00119, HG01498, HG00275, NA18853, HG00183, HG01522, NA19350, HG01462, NA18908, NA19473, NA20806, HG01377, HG00143, HG00336, NA20502, HG00272, HG00271, NA19779, HG00136, HG01067, HG01198, NA20281, HG01515, HG00152, HG00734, HG01518, HG00536, NA11930, NA07037, NA20278, NA20809, NA20503, HG01072, HG00100, NA18561, NA18933, NA19404, HG00127, HG01055, HG01342, HG00731, HG00245, HG00736, NA19003
Known GenesCREB5
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1189e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss297
Observed Complex0
Frequencyn/a


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