A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1282e199



Internal ID22759055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39373726..39529923hg38UCSC Ensembl
chr8:39231245..39387442hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38156198
hg19156198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2662293, esv2675237, esv2663438, esv2666583
SamplesNA20588, NA12383, HG00189, NA20761, HG00442, HG00143, HG00608, HG00142, NA20766, NA20508, NA19664, NA10851, HG00559, NA19399, NA12273, NA20783, NA12414, NA20514, NA12843, NA11920, HG00257, HG01066, HG00151, HG00233, NA20512, HG00181, NA12340, NA19684, NA18530, HG00737, HG00115, NA20517, HG01461, NA20771, NA12750, NA12399, NA20806, HG01522, NA18627, HG00337, HG00271, NA12813, NA07346, HG00138, HG00122, NA20589, HG01351, NA19678, NA18558, HG01492, NA07048, NA07347, NA20768, HG01083, HG01365, HG00185, HG00243, HG00158, HG00281, NA20759, NA12275, HG01069, NA19720, HG01080, NA20518, HG00148, NA20775, NA12156, HG01519, NA20812, HG00325, HG00232, NA12044, NA11994, NA19722, HG00160, NA18985, NA20757, HG00323, HG01550, HG00253, NA20515, NA19789, NA20755, NA18539, HG00137, NA12777, HG00154, NA20800, HG00268, HG00266, HG00282, HG00245, NA20521, HG01095, HG00657, NA20810, NA20760, NA19663, NA12718, NA20519, NA18534, HG00239, HG00740, HG01047, NA20525, NA19654, HG00324, NA11919, HG00651, HG00690, HG00531, NA20581, NA12829, NA11893, HG00684, NA19750, HG00140, HG01497, HG01334, HG00146, NA19682, NA12144, NA12778, HG00246, HG00126, NA12546, HG01107, HG01075, NA12043, HG01148, HG00258, HG00155, HG00254, HG00336, HG00625, NA19747, NA12272, HG00734, HG01357, HG01174, NA20790, NA20530, NA20527, HG01375, NA20792, NA20778, NA19679, HG01113, NA20544, HG01137, NA19783, NA12763, HG00418, NA18610, HG01342, NA12347, NA06994, HG00513, HG00478, NA19785, HG00259, NA19779, NA19716, HG00267, NA19474, HG00310, HG00112, NA19770, NA20826, HG00377, NA11892, HG01125, NA12006, NA18623, NA20585, NA12154, HG01437, HG00581, HG01516, HG00096, HG00114, NA11830, HG01521, HG01098, HG01356, NA20543, HG00536, NA11829, HG00361, HG01052, HG00187, HG00100, HG01188, NA11933, HG01389, HG00306, NA12045, HG00640, HG00318, NA18486, HG01465, HG00699, NA12004, NA20805, NA19777, NA18596, NA12058, NA20808, HG00177, NA18526, NA12400, NA12155, HG01140, NA12413, NA12341, HG00327, NA20537, NA18967, NA19746, HG00127, NA19381, HG01366, HG01070, HG00251, NA19762, NA19728, NA19448, HG00702, NA20586, HG00173, NA19723, NA12891, NA20769, NA12348, NA18942, HG00736, NA11992, HG01354, NA20540, NA12287, HG00247, HG00369, HG00270, NA20513, HG00590, NA20541, HG01134, NA12282, NA19651, HG01067, NA20819, HG01170, HG01495, NA19719, HG01072, HG01176, NA12889, HG01440, HG00182, NA20811, NA19725, HG00637, HG00338, HG00159, NA12828, HG00178, NA20533, HG00530, NA18638, HG00464, HG00108, HG00260, NA20818, NA11831, NA10847, HG01353, HG00543, HG00313, HG00133, HG00188, HG00149, HG00560, NA19657, HG01360, HG01187, NA20787, HG01384, HG00328, NA20505, HG00428, HG01515, NA20536, HG00475, HG00320, HG00500, NA19788, NA20506, NA20770, HG00635, HG01073, HG00273, HG00373, HG01197, NA20538, NA12249, HG00117, NA12827, HG00276, NA20828, NA19756, HG00141, NA18536, NA20542, NA20534, NA19675, HG01204, NA20765, NA20526, NA20522, NA20801, NA12716, NA18535, NA18952, NA12775, NA19749, NA18950, HG00375, HG01253, HG00136, HG00638, NA20804, HG00278, NA07051, NA12046, HG01494, NA19786, NA20516, HG01108, NA20803, NA20797, HG00256, NA06986, HG00125, NA19759, NA19376, NA19078, HG00672, HG00111, HG00578, HG00312, NA20582, HG00329, HG00656, HG01254, HG01055, HG00174, HG00123, NA12830, HG00186, NA20807, HG00131, NA19726, HG01251, NA19661, HG01377, HG01378, NA19755, HG00345, HG00554, HG01191, NA20509
Known GenesADAM3A, ADAM5
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1282e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss372
Observed Complex0
Frequencyn/a


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