A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664537



Internal ID9930642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:138282583..138283032hg38UCSC Ensembl
chrX:137364742..137365191hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38450
hg19450
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5972542, essv6491178, essv6571079, essv6134724, essv5652397, essv6372327, essv5874992, essv5988927, essv5632540, essv6434873, essv5845276, essv6225421, essv6386403, essv6548173, essv5836438, essv5964599, essv5730721, essv6224067, essv5981795, essv5572036, essv6146166, essv5614111, essv6255598, essv5889876, essv5779120, essv5651364, essv5620490, essv5879305, essv5478447, essv5987709, essv6357876, essv5998961, essv6079947, essv5841154, essv6287568, essv6460264, essv5398258, essv6506491, essv5799830, essv6061270, essv6061227, essv6246848, essv5956777, essv5938052, essv5663973, essv6292185, essv6512467, essv6146491, essv5671335, essv6124120, essv5840318, essv6523320, essv6310712, essv6514067, essv6198272, essv6227204, essv5830475, essv5587312, essv5845560, essv6329547, essv6228689, essv6409557, essv5721934, essv5451127, essv5812887, essv6118107, essv5613495, essv6532613, essv6598048, essv6341189, essv5816740, essv5969223, essv5712146, essv5876621, essv6497855, essv5896274, essv6527668, essv6273217, essv5464009, essv6330316, essv6164479, essv6280549, essv5815940, essv5570836, essv6085558, essv5866009, essv6196828, essv5953573, essv5818968, essv5403809, essv6346385, essv5743880, essv5608315, essv6274445, essv5512355, essv6597643, essv6345606, essv5944412, essv6303194, essv6280691, essv6399095, essv6065042, essv5460531, essv6507351, essv5587919, essv5502025, essv5644513, essv6433143, essv6244446, essv6204038, essv6014324, essv5967644, essv6437097, essv5589441, essv6169684, essv6142128, essv5901662, essv5990972, essv5966035, essv5645615, essv5584450, essv6558222, essv6016486, essv6093421, essv6051096, essv5788720, essv5772323, essv5404652, essv6082281, essv6521335, essv5486088, essv5417775, essv6039782, essv6149129, essv6003909, essv5402397, essv6427915, essv5453379, essv6163909, essv5418709, essv5781793, essv5651573, essv5773148, essv5490406, essv5476368, essv6572288, essv6108012, essv6038232, essv5503710, essv6103728, essv5738694, essv6530154, essv5480999, essv6354402, essv6208251, essv6014583, essv5892918, essv5593666, essv5845917, essv6322528, essv5915613, essv6005354, essv5443069, essv5456855
SamplesNA19700, NA19703, HG00608, NA18621, HG00671, NA18592, NA19399, HG00187, NA18565, NA18561, NA11933, NA18599, NA18999, NA18603, NA18596, HG00566, NA18530, NA18606, NA18526, NA12400, NA18633, NA18602, NA18627, NA18563, NA19396, NA19381, HG01350, NA19379, NA18550, HG00122, NA18597, NA18489, NA20798, HG01351, NA18595, HG00702, NA18635, NA18567, NA18619, NA19916, NA18558, HG00634, NA12283, HG01354, NA19088, NA18571, HG01083, NA18498, NA19782, NA18964, HG00537, NA19079, NA18611, NA19651, HG01067, HG00683, HG00236, HG01072, HG00534, HG00705, NA19087, HG00309, NA19002, NA18990, NA18520, HG00159, NA18557, NA18539, NA18638, HG00464, NA19007, NA18614, HG00313, HG00133, NA18544, NA18605, NA18538, HG00268, HG01187, NA19070, HG00596, HG00328, NA19077, NA19462, HG00190, HG00653, HG00657, NA19391, NA18637, NA18572, NA18534, NA18630, HG00619, NA18548, HG00740, HG01047, HG01102, HG00324, NA18626, HG00479, NA18912, HG00157, NA18553, HG00276, NA18963, NA18536, NA19625, NA18634, NA18593, NA19675, NA18541, NA18546, NA20296, NA18608, NA19375, HG00258, NA18632, NA18542, NA19440, NA18543, NA18559, NA18564, NA19072, HG00638, NA19010, NA12046, HG01174, HG01494, NA19439, NA19324, HG01113, NA19083, HG00662, NA19085, NA18615, HG00620, HG00672, HG00614, HG01491, HG00312, NA18631, HG00656, NA19713, NA18636, NA18609, HG00186, HG00112, NA19770, NA19080, NA18552, HG00377, HG00372, HG00595, NA19004, NA18624, NA18623, NA12154, HG01097, NA18612, NA18549, NA18622, HG01061, HG00437, NA18620
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664537
Frequency
Sample Size1151
Observed Gain0
Observed Loss164
Observed Complex0
Frequencyn/a


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