A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv545e199



Internal ID18982599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:36181069..36227348hg38UCSC Ensembl
chr17:34508445..34554792hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3846280
hg1946348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2666825, esv2676887, esv2660470, esv2657701
SamplesHG01441, NA11881, HG00309, HG00157, NA12154, NA12489, HG00252, HG01440, NA07347, NA20787, HG00257, HG00182, NA20527, NA12286, NA12342, HG00328, NA20752, HG01173, NA20510, HG00112, HG00274, HG00186, NA12347, HG00131, NA20544, NA20796, NA20535, HG00155, HG00160, NA11918, NA10847, HG01389, NA20759, HG01197, HG01051, HG00189, NA20800, HG01082, HG01488, NA12828, HG01174, HG00148, HG01350, NA20539, HG00187, NA07051, HG00280, HG00335, HG01168, HG00177, NA20798, HG00319, HG00737, NA12287, NA20521, NA20803, HG00156, HG01171, HG00353, HG00269, HG00554, NA12414, HG01107, HG01550, HG00158, HG01148, NA20505, HG00242, NA11919, NA12763, HG00346, HG01384, HG01456, NA20819, NA12282, NA20515, NA12004, HG00337, HG01378, NA11994, NA20811, HG00140, HG00638, NA12155, HG00180, HG00259, HG00096, NA07357, NA20757, HG01048, HG01061, NA20530, HG00372, HG01183, HG01495, NA20801, NA20807, NA20754, HG01124, NA12273, HG00315, NA07048, NA12761, HG00149, HG00338, NA11933, NA20541, HG00150, NA20765, HG00178, HG00125, HG00258, NA11843, NA11831, NA12829, HG01113, HG01136, NA11894, NA12400, NA20520, HG00264, HG01253, NA11995, HG00174, HG00637, HG00243, HG00254, HG01187, NA12830, NA12777, HG00357, NA20589, HG00237, HG00343, NA12144, HG00133, HG00114, NA12751, HG01497, NA12006, HG00306, HG00373, HG00159, HG00267, HG01437, HG00124, HG01097, NA07346, NA12046, HG00108, NA12716, HG00233, HG01516, NA20536, HG00268, HG00640, HG01066, NA20760, NA20512, HG00732, NA12778, NA12348, NA20790, HG00185, NA20795, NA20826, HG00263, NA06986, NA20753, HG00176, HG00260, NA20540, HG01073, HG00239, HG00265, HG00273, HG00282, HG01170, HG00232, HG01069, HG01176, NA20814, HG00249, NA20818, NA11892, HG00116, HG00277, NA20774, NA20828, HG00103, HG01080, NA20815, HG00740, NA20797, NA20542, NA20582, HG00329, NA20766, HG00246, NA12283, HG01060, HG01383, HG00236, HG01149, HG00120, HG00151, NA11832, NA10851, NA20525, NA20581, NA20537, HG01190, NA20534, NA12272, NA20756, HG01095, HG00181, NA12749, NA20799, NA06984, NA12413, NA20518, HG00138, NA12156, NA12889, HG00262, HG01112, HG00118, NA20509, HG01390, NA20507, NA20513, NA11830, NA11992, NA12003, NA20810, HG00123, HG00281, HG00285, NA11993, NA12399, NA20812, NA12842, NA20543, HG01251, HG00367, NA12045, NA20792, HG01125, NA11829, HG00251, NA20768, HG00119, HG00320, HG00275, HG00324, NA12717, NA20528, HG00641, HG00183, HG01522, HG00137, HG01102, HG01489, NA20804, HG00336, NA20502, NA20517, NA20772, HG00345, NA20538, HG00271, NA20519, HG00136, HG00126, NA07000, NA12775, HG01067, HG01354, HG00312, HG00327, HG01198, HG00323, NA12827, HG01515, HG00313, NA12043, HG00152, HG01359, HG00318, NA12750, NA20514, NA12748, NA11930, NA20522, NA20809, NA20503, NA20526, HG00344, HG01072, NA20785, HG01052, HG00100, NA20506, HG00127, NA07056, HG01342, NA20516, HG00731, HG00245, HG00736, NA20508, HG00310, HG00261, HG01098, NA06989, NA12340, NA20775, NA11931, NA12813, HG00117, NA20808, NA20816, HG00326, HG01491, NA20778, NA20786, HG00270, HG00553, HG00190, HG01182, HG00122, HG00106, NA20588, HG01188, HG01204, NA12776, HG01461, HG00146, NA12341, HG00188, NA20586, HG00247, HG01521, HG00256, NA20770, HG00342, HG00244, HG00266, NA20532, HG00115, HG00154, HG00321, HG00339, NA20533, HG00179, HG00250, HG01140
Known GenesCCL3L1, CCL3L3, CCL4L1, CCL4L2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv545e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss358
Observed Complex0
Frequencyn/a


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