A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv189e199



Internal ID22757962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5762715..5788262hg38UCSC Ensembl
chr11:5783945..5809492hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3825548
hg1925548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2667023, esv2669166, esv2660528
SamplesNA20509, NA19394, NA19701, NA20761, HG00542, NA12717, NA19058, NA12842, NA19703, HG01462, HG00608, NA18621, NA20766, NA12286, NA20508, NA19664, HG00671, NA10851, NA12273, NA20783, NA18565, NA12843, NA11931, HG01066, HG00315, NA12751, NA19355, NA20332, NA19377, NA18959, HG00737, HG00449, HG00654, NA19443, NA19920, HG00261, NA18510, NA12750, NA18602, HG01522, NA19107, HG00663, NA19446, HG00138, NA19373, NA18940, NA18519, HG00589, HG00272, NA20798, HG01351, HG01177, NA19678, NA20756, NA20795, NA18574, HG01083, HG01365, HG00334, HG00185, HG00243, NA19130, NA19079, HG00158, NA11930, HG00512, HG00281, HG01080, NA20518, HG00335, HG00325, HG00232, NA19372, NA11994, NA19235, NA19172, NA19722, HG00160, NA18990, NA19239, NA18985, NA20342, HG00326, NA20757, NA20127, NA19985, HG00253, NA20753, HG01124, HG00137, NA18951, NA18605, HG00731, HG00266, HG01171, HG00380, HG00282, NA19070, NA19403, NA18933, NA20521, HG00657, NA20760, HG00368, NA20314, HG00344, HG00263, NA12718, NA20519, NA18871, NA18572, NA18534, HG00692, NA18907, NA19654, HG00324, NA19461, HG00404, HG00479, NA06989, HG01101, NA18553, NA19761, NA19009, HG00152, HG00146, NA18963, NA19682, NA12144, HG00463, NA12778, NA18570, HG00126, NA19625, HG01107, HG01075, HG01148, HG00611, NA18632, NA19652, HG00155, NA19440, HG00336, NA20276, NA19434, NA18564, NA19747, NA18628, NA20815, NA12272, NA19444, NA20520, NA19010, HG00098, NA20530, NA20527, HG00237, NA19679, NA19428, NA19311, HG01113, HG01137, HG00116, NA18610, NA12347, HG00339, NA18501, HG00614, HG00478, HG00259, NA19779, HG00342, HG00267, NA20510, NA18609, NA18873, HG00112, NA19770, HG00280, NA19780, NA19900, HG00377, NA20503, HG00147, NA19129, HG00171, NA20585, NA20754, NA19429, HG00581, NA18577, NA18620, HG01060, HG00114, NA19648, HG01098, HG00536, HG00249, NA19466, NA11995, HG00361, HG00524, HG00187, NA18507, NA11933, NA18599, HG01374, HG00306, HG00318, NA18486, HG00699, NA12004, NA19777, NA19057, NA18596, HG01456, NA18606, HG00179, HG00177, NA20507, NA18870, NA12155, HG01140, NA12413, NA12341, HG01250, NA19746, NA19396, HG00127, NA19660, NA20796, NA19005, NA19382, NA18489, NA19448, HG01488, HG00702, HG00173, NA19198, NA18619, HG00330, HG00634, HG00736, NA19197, HG01354, NA19313, HG00369, HG00270, NA20513, NA18611, NA19404, NA12761, HG01134, NA12282, HG00277, NA19651, HG01067, HG00120, NA19383, NA18874, HG00106, HG00236, NA19137, NA20340, NA19371, NA18560, NA19731, NA19075, NA18617, NA19471, NA19159, HG00309, HG00182, HG00427, NA19189, NA12828, NA19456, HG00178, NA20533, NA18908, NA18638, HG00739, NA11993, HG00464, HG00108, HG00260, NA20818, NA18614, HG01353, HG00543, HG00313, HG01183, HG00188, NA18544, HG00560, NA19247, NA18613, HG01187, NA19707, NA18934, HG00596, HG00145, HG01384, HG00328, NA19077, NA12003, HG00428, NA19462, HG00653, HG00701, HG01515, NA20536, NA19236, HG00533, NA20506, NA20126, NA19658, NA20344, HG00619, HG00635, HG01094, NA20299, NA19655, HG01197, NA18499, HG00117, HG00613, HG00321, NA18853, HG00276, NA19225, NA20828, HG00141, NA18634, NA20534, NA19675, HG01204, NA18576, NA20765, HG00124, NA20801, NA12716, HG00119, HG00285, NA18950, HG00375, HG00357, HG01253, NA19435, NA20804, NA19773, NA20785, NA20504, NA19786, HG00319, HG01108, NA20803, NA20797, HG00256, NA06986, HG00269, NA19818, NA19759, HG00111, HG00578, NA19248, HG00312, NA19472, NA19060, HG00329, NA12749, NA19713, HG01254, NA20807, HG00131, NA19726, NA18552, HG01251, NA19755, NA20322, NA18511, HG01097, HG00554, HG00180, HG01061, NA12776
Known GenesOR52N1, OR52N5
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv189e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss386
Observed Complex0
Frequencyn/a


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