A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv879e199



Internal ID22758652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:111524698..111530945hg38UCSC Ensembl
chr3:111243545..111249792hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg386248
hg196248
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2656762, esv2669248
SamplesNA20588, NA18502, HG00189, NA19701, NA12717, NA19058, NA12842, NA18621, HG00142, NA20766, NA20508, NA19664, NA18508, NA19399, NA12273, NA20514, NA11931, HG00257, HG00151, NA20816, NA20752, HG00244, NA12751, NA20332, NA18959, NA20356, NA19920, HG00261, NA20771, NA18510, NA12750, HG00693, HG00337, NA19107, NA12813, NA20814, NA19446, NA07346, HG00138, NA19171, NA19379, HG00272, HG00122, NA19315, NA20589, NA20774, NA20756, HG01492, NA07048, HG00334, NA19904, NA19384, HG00243, NA20291, NA19130, HG00158, HG00139, HG01069, NA19720, NA20518, HG00335, HG00148, NA12156, HG00156, NA20812, NA18868, HG00325, NA11932, HG00232, NA12044, NA11994, NA19235, NA19722, HG01198, NA18557, NA20342, HG00326, NA20757, NA18867, HG00253, NA20515, NA19789, HG01124, NA12777, NA19908, NA12489, NA20800, HG00443, HG01171, NA19403, HG01095, NA19717, NA19455, NA19663, HG01498, HG00263, HG00275, NA18871, NA19654, NA11919, HG00331, HG01497, NA19452, NA12144, HG00463, NA19318, HG00126, NA18858, HG01075, NA12043, HG01148, HG00258, NA19729, NA19256, HG00625, NA18564, HG00353, NA20815, HG01551, HG01357, HG01174, NA20530, NA20527, NA19835, NA20792, NA19324, HG01113, HG01137, HG00116, NA19360, NA12347, NA18501, NA19785, NA18631, HG00259, NA19223, NA19779, NA19474, NA20289, HG00112, NA20758, NA19080, NA20826, NA19780, NA19711, HG00377, NA19430, NA11892, HG01125, NA19463, NA12154, NA20754, NA19429, HG00553, NA19676, HG00626, HG00403, HG00096, HG01060, HG01441, NA11830, HG01098, HG01356, NA19397, HG00249, HG00361, HG00100, NA19704, NA18507, HG01374, HG00103, NA19393, NA19777, HG01456, NA12058, NA20346, HG00177, NA19190, NA19098, NA18870, NA12155, HG01140, NA12341, HG00327, NA20537, NA19374, HG01250, NA19746, NA19396, HG00127, NA19660, NA19381, NA19076, HG01070, NA19382, HG01488, HG00689, HG00173, NA19723, NA19198, NA19916, NA20769, NA12348, NA19131, NA12283, HG01354, NA20540, NA19771, NA19054, HG00270, NA18498, NA19782, NA19681, NA20336, NA20541, HG01134, NA12282, NA19651, HG00120, NA18874, HG00106, HG01170, HG00236, HG01495, NA19917, NA19137, NA20340, NA19385, NA19087, NA12889, HG01440, HG00182, HG00159, NA12828, NA19456, HG00178, NA18908, HG00264, NA11993, HG00464, HG00108, HG00260, NA20818, NA10847, HG00133, HG01183, HG00188, HG00176, NA18934, HG01384, HG00328, NA12342, NA19077, NA19462, NA19347, NA19152, NA19391, NA19327, NA19236, NA18516, NA19982, NA19788, NA20344, HG00708, HG00273, NA19114, NA20299, NA19449, NA19655, HG01197, NA18499, NA12249, HG00321, NA12827, NA20282, NA19257, NA20828, NA18634, NA19436, NA20765, NA18546, NA20526, NA20296, NA19685, NA19401, HG00124, NA20801, HG00119, NA11881, NA19108, NA12775, HG00366, NA19732, NA19435, HG00638, NA07051, NA12046, NA19439, NA20504, NA19467, HG00319, NA20516, NA20803, NA07037, NA06986, HG00125, NA20341, NA19818, NA19248, HG01491, HG00312, NA19472, NA12749, NA20334, HG01055, HG00123, NA12830, HG00186, NA20807, NA19726, NA19213, HG00343, HG01251, HG00372, HG00252, NA07056, NA18505, NA19755, NA19758, NA20322, NA07000, NA18549, NA20509
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv879e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss333
Observed Complex0
Frequencyn/a


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