A curated catalogue of human genomic structural variation

Variant Details

Variant: dgv545e199

Internal ID20123847
Location Information
TypeCoordinatesAssemblyOther Links
chr17:36181069..36227348hg38UCSC Ensembl
chr17:34508445..34554792hg19UCSC Ensembl
Allele length
AssemblyAllele length
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
AnalysisNo reference, merging analysis
Pubmed ID23128226
Accession Number(s)dgv545e199
Sample Size1151
Observed Gain0
Observed Loss358
Observed Complex0

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