A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672726



Internal ID9938831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:106110005..106112772hg38UCSC Ensembl
chr3:105828852..105831619hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg382768
hg192768
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5881869, essv5396773, essv5897730, essv6042973, essv6283616, essv6398188, essv6588791, essv6228151, essv6597155, essv6079488, essv5897988, essv5810166, essv5529592, essv5677499, essv5551130, essv5737725, essv6086848, essv6375855, essv6271801, essv5748945, essv6551049, essv6201399, essv6564888, essv5733370, essv5834946, essv6370462, essv5739531, essv6177449, essv5402544, essv6192133, essv6423765, essv5450573, essv5967663, essv6201063, essv5680948, essv5859392, essv5873035, essv5809012, essv6177314, essv5626873, essv6277007, essv5756860, essv6090699, essv5496239, essv6559090, essv6005162, essv6270775, essv6329075, essv5659990, essv6512306, essv6336802, essv5591647, essv5884904, essv5700727, essv6211484, essv5647473, essv6206800, essv5595745, essv5678527, essv5456568, essv6145816, essv5512850, essv5950475, essv6558811, essv5585350, essv6378314, essv5544350, essv6577888, essv6309754, essv5450606, essv5937644, essv5754999, essv5636111, essv5992313, essv5652876, essv5833911, essv6495609, essv6122149, essv6134198, essv5540087, essv6555965, essv5607252, essv5503335, essv6564918, essv5753671, essv5409405, essv5847099, essv6371377, essv6416539, essv6365407, essv6290298, essv5442481, essv6192108, essv5692838, essv6357737, essv6023076, essv5532498, essv5429371, essv6588142, essv6375531, essv5620433, essv6234882, essv6052684, essv6172185, essv6506212, essv6311460, essv5729635, essv5689973, essv6007771, essv6177469, essv6079640, essv5714092, essv5494858, essv6508806, essv6286358
SamplesNA18502, HG01060, HG00114, NA12717, HG01173, NA20529, HG00143, NA19397, NA11829, NA19204, NA18508, HG00187, HG00257, NA20802, HG00367, HG00244, HG00103, NA20808, HG00177, HG00261, NA07357, HG00271, NA12813, NA18967, NA19746, NA19396, HG01070, HG01168, NA19131, NA11992, NA07347, NA19457, HG01083, NA20287, NA19681, NA12761, NA20539, HG01069, HG00335, NA12156, NA06984, NA18868, HG00262, NA18560, NA12044, NA19207, NA19172, HG00309, HG00182, NA19901, NA19239, HG00326, NA20533, NA18867, HG00253, NA20755, HG00133, NA12489, HG00731, HG00268, HG00266, NA12003, HG00732, NA20760, NA18516, HG00344, NA20126, NA19776, NA18907, HG00324, NA11919, NA11894, NA18532, HG00140, NA12827, NA12144, NA18523, NA19469, HG01107, NA18974, NA19375, NA12716, NA11881, HG00336, NA19321, NA19108, NA18517, HG00734, NA19240, HG01174, NA20527, HG00237, NA20504, NA20544, HG00319, HG01108, NA19360, HG00256, NA12763, NA12347, NA06994, NA18971, HG00267, NA19713, NA19093, HG00174, HG00123, NA19102, NA18873, NA20758, NA20826, HG00343, NA18505, NA12154, NA20509
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672726
Frequency
Sample Size1151
Observed Gain0
Observed Loss115
Observed Complex0
Frequencyn/a


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