A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623126



Internal ID6663294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46159786..46227801hg38UCSC Ensembl
chr10:47531022..47599037hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3868016
hg1968016
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv120e214
Supporting Variantsessv13785566, essv13785502, essv13785506, essv13785571, essv13785435, essv13785466, essv13785491, essv13785463, essv13785472, essv13785534, essv13785444, essv13785512, essv13785567, essv13785453, essv13785501, essv13785558, essv13785562, essv13785519, essv13785437, essv13785480, essv13785544, essv13785557, essv13785542, essv13785538, essv13785429, essv13785551, essv13785464, essv13785543, essv13785556, essv13785503, essv13785455, essv13785513, essv13785521, essv13785545, essv13785572, essv13785443, essv13785477, essv13785525, essv13785568, essv13785458, essv13785424, essv13785570, essv13785483, essv13785481, essv13785456, essv13785479, essv13785445, essv13785517, essv13785514, essv13785500, essv13785537, essv13785465, essv13785448, essv13785553, essv13785484, essv13785428, essv13785462, essv13785549, essv13785486, essv13785454, essv13785440, essv13785511, essv13785523, essv13785536, essv13785478, essv13785470, essv13785552, essv13785526, essv13785460, essv13785485, essv13785433, essv13785482, essv13785520, essv13785449, essv13785494, essv13785471, essv13785533, essv13785550, essv13785488, essv13785498, essv13785507, essv13785474, essv13785527, essv13785515, essv13785529, essv13785432, essv13785508, essv13785565, essv13785518, essv13785510, essv13785555, essv13785493, essv13785490, essv13785459, essv13785495, essv13785559, essv13785441, essv13785563, essv13785439, essv13785457, essv13785499, essv13785509, essv13785564, essv13785427, essv13785528, essv13785505, essv13785535, essv13785450, essv13785547, essv13785476, essv13785561, essv13785522, essv13785431, essv13785548, essv13785532, essv13785430, essv13785560, essv13785569, essv13785546, essv13785434, essv13785451, essv13785497, essv13785467, essv13785468, essv13785452, essv13785438, essv13785554, essv13785492, essv13785447, essv13785473, essv13785531, essv13785496, essv13785540, essv13785504, essv13785539, essv13785516, essv13785446, essv13785425, essv13785489, essv13785461, essv13785442, essv13785541, essv13785530, essv13785487, essv13785475, essv13785469, essv13785436, essv13785524, essv13785426
SamplesHG00096, HG01485, HG01413, NA19141, HG01098, NA19794, NA10851, NA12273, HG03237, HG01537, HG03753, HG02836, HG04076, HG00244, HG04094, HG01465, NA19355, NA20332, NA18959, HG00177, NA20507, HG03139, HG01632, HG01461, HG00271, NA12813, HG03464, HG01506, NA21135, NA18940, NA18550, HG00109, HG03135, NA20798, NA20890, HG02952, HG01997, HG01676, NA20317, NA07048, HG01354, NA19771, HG02054, HG03224, NA19922, HG03209, HG00139, HG01398, HG02224, HG01628, NA18868, HG04106, HG03691, NA18748, HG02471, HG01405, HG03380, NA19239, HG01121, NA20757, HG03585, HG02477, NA20318, HG00188, NA20904, NA18951, HG02570, HG02439, NA19908, HG00731, HG03132, HG01360, HG00982, NA19707, NA20787, NA18934, HG03787, NA12342, HG01669, HG00360, HG01344, HG00368, HG02450, HG01989, HG02508, NA18948, HG02757, NA21116, NA19461, NA20903, HG03660, HG00531, HG00684, HG04155, HG00117, NA19338, HG01890, HG01708, NA12778, HG02586, HG03694, NA18546, HG03064, NA20799, HG04188, HG02807, HG00254, NA19321, NA18543, HG02501, NA19747, HG01131, HG00742, HG00353, HG02696, HG01878, NA19037, HG00278, NA20520, NA12046, NA20362, HG02982, HG01205, NA19324, NA20803, HG02019, HG03103, HG00672, HG02095, NA12749, HG03863, HG01783, HG00343, HG03538, HG02051, NA18957, NA07056, HG02861, HG02855, NA18624, HG02805, HG01886, HG01672, HG03129, NA20908, HG03686, HG01695, HG03271, HG02760
Known GenesANTXRLP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623126
Frequency
Sample Size2504
Observed Gain149
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer