A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1266e199



Internal ID22759039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:8204623..8230570hg38UCSC Ensembl
chr8:8062145..8088092hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3825948
hg1925948
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2662425, esv2676673, esv2671947, esv2661577, esv2673876, esv2659103
SamplesHG00650, HG00542, NA19058, HG00143, HG01462, HG00608, NA18621, NA18947, NA19664, NA19066, HG00242, HG00559, HG00257, HG00315, HG00151, NA18999, HG00233, NA18959, HG00449, HG01461, HG00654, NA18633, NA18602, HG00693, NA18627, HG00271, HG00663, NA18563, HG01350, NA18940, HG00589, HG00122, NA19678, NA18567, NA18558, NA18960, NA18618, NA18574, NA18571, HG01365, HG00334, HG00537, HG00243, NA19079, NA18949, HG00158, HG00512, HG00281, HG00139, HG00335, HG00148, HG00156, HG00325, HG00534, HG00705, NA19722, NA18990, NA18557, NA18985, HG00326, NA19789, NA18539, HG01124, HG00137, NA18951, HG00443, NA18538, HG00266, HG00282, NA19056, HG00557, HG00657, NA19717, NA19663, HG00556, HG00583, NA19081, HG01498, HG00275, NA18579, NA18572, HG01149, NA18948, NA18534, NA18981, HG00692, NA19064, NA18548, NA18537, HG00284, HG00651, HG00250, NA19084, NA18626, HG00690, HG00404, HG00531, HG00479, HG00331, HG00140, NA18553, HG01497, NA19059, HG01334, NA19761, NA19009, NA18555, HG00152, HG00146, HG00704, HG00463, HG00246, NA18570, HG00126, NA18541, NA18953, NA19003, NA19729, HG00611, NA18632, HG00336, HG00625, NA18564, NA19747, NA18628, NA19010, HG01357, HG00237, NA19679, HG01113, HG00116, NA18943, NA19783, HG00662, HG00418, NA18615, NA18610, HG00620, HG00339, HG00614, HG00513, HG00478, NA19785, NA18631, HG00259, NA19779, HG00342, NA19716, HG00267, NA18636, NA18609, NA19770, HG00280, NA19080, NA18983, HG00595, NA18989, HG01125, HG00628, NA18624, NA19063, NA18612, NA19074, HG00581, NA18577, NA18620, HG00593, HG00403, HG00096, HG01441, HG00592, HG01356, HG00249, HG00361, NA18592, HG01359, HG00524, HG00187, NA18980, NA18561, NA18599, HG01389, HG01374, HG00318, HG01465, HG00699, HG00103, NA18545, NA19777, NA19057, HG00566, HG00179, HG00177, NA18526, HG01140, HG00327, NA18967, NA19068, HG01250, NA19746, NA19660, NA19076, NA19005, NA18944, NA18550, HG01366, HG00251, HG00501, NA19762, NA19728, NA18595, HG00702, HG00689, HG00448, HG00173, NA19723, NA18982, HG00330, NA18942, HG00610, HG00346, HG01354, NA19771, HG00247, NA19054, HG00369, HG00270, NA19782, NA19681, HG00590, NA18611, HG01134, HG01455, NA19651, HG00120, HG00683, HG00236, NA18977, HG00262, NA19719, NA19731, NA18617, HG00422, NA18986, NA19087, HG01440, HG00309, HG00182, NA19002, HG00427, HG00338, HG00159, HG00530, HG00264, HG00464, HG00108, HG00260, NA19007, NA18614, HG00543, HG00313, HG00133, HG01136, HG00188, NA18544, HG00560, NA18613, HG00629, NA19657, HG01360, HG00176, NA19082, HG00596, HG00328, HG00428, HG00653, HG00577, NA18956, HG00701, HG00475, HG00436, HG00584, HG00533, NA18637, HG00500, NA19788, NA18976, NA18630, HG00619, HG00708, HG00635, HG00273, NA19774, NA19000, NA19655, HG00117, HG00613, HG00525, HG00321, NA19756, NA18536, NA18634, NA19675, NA18945, NA18576, NA18546, NA18608, HG00476, HG00124, NA18542, HG00119, NA18535, NA18961, NA18543, NA19749, HG00565, HG00366, HG00375, HG00357, NA19732, HG01253, HG00136, NA18941, NA19773, HG00607, HG00319, HG00256, NA19085, HG00269, HG00125, NA19078, HG00707, HG00672, HG00111, HG00578, NA19060, HG00329, NA18987, HG01254, HG00186, HG00131, NA19726, NA18972, HG00343, HG00372, HG01377, HG00472, HG01378, NA19755, HG00345, NA18549, HG00180, NA18622, HG00437, NA18562, NA18965
Known GenesFAM86B3P
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1266e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss356
Observed Complex0
Frequencyn/a


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