A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv175e199



Internal ID22757948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:131110795..131114516hg38UCSC Ensembl
chr10:132909058..132912779hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg383722
hg193722
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2669390, esv2658017
SamplesNA20588, HG00189, NA20761, NA12717, HG00442, NA20529, NA12842, HG00143, NA19703, NA18621, HG00142, NA18947, HG00242, HG00559, NA12273, NA20783, NA18565, NA12414, NA11931, HG00257, NA20816, NA20752, NA18999, HG00233, HG00244, HG00181, NA18530, NA18959, HG00737, HG01518, NA20517, HG01461, HG00654, NA19067, NA18602, HG00693, NA18988, NA18627, NA19107, NA12813, NA07346, HG00641, HG01350, NA18940, HG00272, HG01177, NA19678, HG01168, NA18567, NA20795, HG01492, NA18618, NA19062, NA18574, NA11918, NA20768, HG00185, HG00311, HG00243, NA19079, NA18949, HG00158, HG00281, HG00335, NA20775, HG00156, NA20812, HG00232, HG00534, HG00705, NA19722, HG00160, HG00118, HG01198, NA18985, HG00326, HG00253, NA20515, NA19921, NA20753, HG00137, HG00731, HG00443, NA18538, HG00266, HG00282, NA19070, NA19056, HG00557, NA12878, NA20521, HG00657, NA20760, HG00368, HG00556, HG00275, NA12718, NA20519, NA18572, NA18948, NA18534, HG00239, NA18981, HG00692, NA19064, NA18548, NA18537, NA19654, NA18573, HG00651, HG00250, NA19084, NA18626, HG00690, HG00404, HG00531, HG00479, HG00350, HG00684, NA19453, NA18912, NA18553, NA19059, NA19761, NA19009, NA18555, HG00152, HG00146, NA18963, HG00704, NA19682, NA18523, HG00126, NA18593, NA12546, NA18974, NA18953, HG01148, HG00258, NA18632, HG00155, NA19440, NA18533, HG00625, NA18628, NA19072, HG00580, NA12272, NA20520, NA19010, NA20527, HG00237, NA19360, HG00662, HG00418, NA18615, HG01489, NA12347, HG00614, HG00513, NA18631, HG00259, NA19779, HG00342, NA19468, NA20510, NA18609, NA18873, HG00112, HG00280, NA11843, NA20758, NA20826, NA19780, NA18983, HG00377, HG00595, NA11892, HG01125, HG00628, HG00171, NA18968, NA19065, NA18612, HG01437, NA18577, NA20772, NA19676, NA18620, HG00626, HG00403, HG00114, HG01098, NA19055, HG00249, HG00524, NA18980, HG00100, NA18599, HG01389, HG00306, NA19092, HG00699, NA20805, NA12058, NA18606, HG00177, NA20507, NA12155, NA07357, NA12341, NA19068, HG01250, HG00127, NA19381, NA19076, NA18944, HG01366, HG00251, NA19382, NA18595, HG00702, HG00689, HG00448, NA20586, NA18982, NA18635, NA18619, NA12891, NA19916, HG00458, NA12348, HG00634, NA18942, HG00610, NA11992, HG01354, NA20540, NA12287, HG00247, HG00270, NA19782, NA19681, NA18964, HG00590, NA20541, NA18611, NA12282, NA12005, HG00683, HG00106, NA20819, NA06984, HG01072, NA18560, NA19075, NA18617, NA18986, NA19087, NA12889, HG01440, HG00182, NA19002, HG00427, NA19901, NA19189, HG00637, NA19445, NA18975, HG00178, NA18973, HG00530, HG00264, NA12748, NA11993, HG00464, NA20818, NA18614, NA11831, HG00149, NA19210, HG00629, NA19657, NA19082, HG01187, HG00596, NA20524, HG01384, HG00328, NA12342, NA19077, NA12003, HG00701, HG01515, NA20536, NA18991, HG00436, HG00320, NA18637, NA19788, NA20506, NA20126, NA18910, NA18976, NA18630, HG00619, HG00708, HG00635, HG00273, NA19774, NA19000, NA19655, HG00373, NA20538, NA12249, HG00525, HG00321, NA18853, HG00141, NA18536, NA20542, NA18634, NA19675, NA18546, NA18608, NA20773, NA20522, NA12716, NA11881, HG01190, HG00285, NA19834, NA19108, NA12775, NA18950, HG00375, HG00357, HG00136, HG00638, NA20804, NA19380, NA07051, NA20785, HG00607, HG00319, NA20516, NA07037, NA19085, HG00125, NA19078, HG00707, HG00312, HG00421, HG00329, NA18987, HG00656, HG00174, HG00123, NA18972, HG00252, HG01378, NA19004, HG01082, HG00345, NA07000, HG01112, HG01191, HG00180, NA18622, NA18562, NA18965
Known GenesTCERG1L
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv175e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss371
Observed Complex0
Frequencyn/a


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