A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1107e199



Internal ID22758880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32548818..32574115hg38UCSC Ensembl
chr6:32516595..32541892hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3825298
hg1925298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2673467, esv2668321
SamplesNA20588, HG00189, NA20761, NA12717, HG00442, NA12842, HG00671, NA18861, NA18508, NA19399, NA20783, NA12414, HG00315, NA20816, NA20752, HG00181, NA20294, NA20332, NA19684, NA19377, HG01461, NA19920, HG00261, HG01522, NA18627, HG00337, HG00271, NA20814, HG00138, NA19373, NA19379, HG00589, HG00272, NA19319, NA19315, HG01351, NA20774, NA18923, NA07347, NA18582, NA18571, HG00334, HG00281, NA20759, NA19720, HG00335, NA18868, HG00325, HG00232, HG00326, NA20515, NA19789, NA18539, NA19921, HG00154, NA18538, HG01171, NA19056, NA19670, HG00245, NA18933, HG00732, HG01095, HG00368, NA18579, HG01149, HG00551, NA19654, HG00284, HG00331, NA19453, NA18912, HG00140, NA18553, HG01497, HG00704, NA19682, NA19395, NA18570, NA18541, HG01075, NA18953, NA20799, NA18632, NA18533, NA19390, HG00336, HG00265, NA19712, HG01551, HG01174, NA20530, NA19835, HG00237, NA19428, NA19324, HG00116, NA19083, NA18943, NA19360, NA19783, NA12763, HG00418, HG00339, NA19328, NA18501, HG00478, NA19223, NA19779, HG00342, NA19716, HG00267, NA19474, NA18609, HG00280, NA20826, NA19711, HG00274, HG01111, NA19316, HG01125, HG00171, NA19065, NA19346, NA19676, HG01516, HG00096, HG01060, NA19648, NA11830, NA19700, NA18924, NA19914, NA19332, NA19704, NA18507, HG00306, HG00367, HG00318, NA19092, NA18486, HG00103, NA19393, NA19777, HG01456, NA20346, HG00177, NA18870, NA18526, NA12155, HG01140, HG00327, NA20537, HG01250, NA19396, NA19660, NA19381, NA20796, NA19005, NA19382, HG00448, HG00173, NA19723, NA19198, HG00330, HG00736, NA11992, HG00247, NA19054, HG00369, HG00270, NA19782, NA12282, HG00277, NA19383, NA19719, NA19385, NA19901, NA19725, NA19189, HG00178, NA18973, NA20818, NA11831, HG01353, HG00188, NA19247, HG00183, HG00176, HG00328, NA12342, NA19347, HG00190, HG00653, NA19327, HG00436, HG00320, NA19788, HG01390, NA18566, NA19000, NA19655, HG00373, HG01197, NA18499, NA20538, HG00117, HG00321, NA18853, NA19338, NA20526, NA20296, NA19685, NA19401, HG00124, NA20801, HG00119, NA18535, HG00285, NA19834, HG00366, HG00357, HG01253, NA19435, HG00278, NA20785, HG00319, NA20803, NA07037, HG00256, HG00125, NA20341, NA19376, NA19398, HG00707, HG00578, NA19248, HG00312, NA20582, NA19472, NA19060, NA20334, HG00174, HG00186, NA19726, HG00343, HG00372, HG01377, NA19755, NA18488, NA19758, HG00345, NA18522, HG01112, HG01191, HG00180
Known GenesHLA-DRB6
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1107e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss256
Observed Complex0
Frequencyn/a


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