A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7883



Internal ID15845795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:32462722..32687666hg38UCSC Ensembl
Outerchr6:32430499..32655443hg19UCSC Ensembl
Outerchr6:32538477..32763421hg18UCSC Ensembl
Outerchr6:32538477..32763421hg17UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38224945
hg19224945
hg18224945
hg17224945
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16514, nssv14185, nssv16664, nssv15271, nssv14165, nssv13480, nssv16904, nssv13450, nssv15943, nssv14120, nssv14579, nssv14027, nssv16673, nssv14005, nssv15548, nssv16281, nssv14628, nssv15338, nssv16800, nssv16544, nssv14614, nssv15519, nssv14287, nssv14866, nssv15369, nssv14674, nssv16341, nssv16643, nssv15066, nssv16740, nssv14538, nssv14065, nssv16033, nssv14270, nssv16221, nssv14135, nssv17070, nssv14508, nssv13151, nssv16197, nssv13181, nssv16063, nssv16227, nssv16257, nssv13390, nssv13945, nssv14806, nssv14195, nssv16784, nssv14698, nssv15279, nssv14222, nssv14848, nssv14699, nssv14265, nssv16980, nssv14035, nssv14147, nssv16153, nssv14669, nssv15036, nssv14878, nssv13792, nssv16017, nssv16191, nssv16401, nssv14180, nssv14946, nssv16574, nssv16694, nssv14215, nssv15549, nssv17190, nssv15913, nssv14598, nssv17010, nssv14609, nssv14240, nssv13975, nssv14155, nssv16347, nssv14377, nssv14267, nssv14237, nssv14207, nssv14276, nssv15672, nssv16814, nssv16123, nssv16634, nssv14716, nssv14060, nssv14036, nssv15006, nssv14673, nssv13852, nssv16874, nssv14030, nssv14347, nssv15309, nssv14125, nssv13882, nssv14257, nssv15702, nssv14639, nssv13976, nssv13039, nssv16934, nssv16994, nssv14728, nssv15368, nssv16890, nssv16213, nssv16047, nssv14838, nssv14295, nssv14210, nssv14117, nssv14608, nssv13942, nssv16950, nssv15518, nssv16003, nssv16077, nssv14312, nssv13330, nssv15308, nssv14216, nssv17024, nssv13997, nssv16251, nssv15399, nssv14478, nssv13219, nssv14568, nssv15642, nssv14729, nssv14227, nssv14154, nssv13540, nssv14448, nssv14819, nssv13702, nssv13009, nssv16317, nssv13249, nssv16137, nssv16243, nssv13912, nssv13271, nssv15488, nssv13822, nssv14836, nssv14578, nssv14686, nssv14638, nssv13189, nssv14658, nssv13915, nssv13672, nssv15241, nssv16333, nssv14126, nssv13211, nssv14252, nssv14688, nssv13732, nssv17130, nssv16830, nssv14849, nssv13061, nssv14066, nssv15339, nssv15126, nssv13241, nssv15458, nssv14064, nssv14057, nssv16303, nssv14808, nssv14177, nssv14156, nssv16311, nssv14668, nssv14105, nssv15398, nssv16844, nssv14150, nssv13309, nssv14317, nssv15459, nssv13510, nssv13885, nssv16703, nssv14976, nssv16287, nssv13279, nssv15973, nssv13360, nssv14006, nssv14703, nssv14467, nssv16604, nssv16273, nssv14186, nssv16167, nssv14325, nssv16920, nssv14818, nssv14282, nssv14355, nssv14718, nssv16964, nssv14437, nssv12979, nssv16161, nssv13121, nssv13159, nssv15612, nssv14192, nssv13129, nssv17160, nssv14124, nssv16371, nssv16484, nssv16183, nssv14245, nssv14548, nssv14896, nssv15489, nssv14644, nssv14246, nssv12949, nssv17040, nssv15732, nssv14162, nssv14793, nssv13069, nssv16860, nssv16724
SamplesNA18502, NA11830, NA18980, NA07029, NA18504, NA12155, NA18563, NA12802, NA18860, NA18942, NA07048, NA10839, NA18975, NA19007, NA10847, NA10863, NA12872, NA18572, NA19221, NA18537, NA18853, NA19132, NA18517, NA18564, NA19240, NA19144, NA12740, NA19173, NA18972, NA18552
Known GenesHLA-DQA1, HLA-DQB1, HLA-DRB1, HLA-DRB5, HLA-DRB6
MethodOligo aCGH
AnalysisStatistical threshold = 5.0, minimum +/- log2 ratio = 0.25 and minimum number of probes = 2
PlatformAgilent-015686 Custom Human 244K CGH Microarray
Comments
ReferencePerry_et_al_2008
Pubmed ID18304495
Accession Number(s)nsv7883
Frequency
Sample Size31
Observed Gain30
Observed Loss25
Observed Complex0
Frequencyn/a


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