A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv456e199



Internal ID22758229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66585107..66586254hg38UCSC Ensembl
chr15:66877445..66878592hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg381148
hg191148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2678069, esv2677015
SamplesNA20588, NA12383, HG00189, HG01173, HG01462, NA12286, NA10851, NA12273, NA12414, NA11931, HG00257, HG00315, NA20512, NA12751, NA12340, HG00115, NA18616, NA20517, NA19443, HG01051, HG00261, HG00337, NA20814, HG00641, HG00138, HG01350, NA19379, HG00589, HG00272, NA20798, HG01351, NA20795, NA18547, NA19062, NA07347, NA18571, HG01365, HG00537, HG00311, HG00243, HG00158, HG00512, HG00281, HG00139, NA12275, HG00335, HG00148, NA20775, NA12156, HG00156, NA11932, NA12044, NA19172, HG00160, HG00118, HG01198, HG01133, NA19789, NA18539, HG01124, HG00137, NA18605, HG00268, HG00282, HG01095, HG00657, HG00344, HG01498, NA12718, NA20519, HG00740, NA18573, NA11919, HG00651, NA19084, HG00479, NA20581, NA12829, NA11893, HG01334, HG00152, HG00146, NA12144, NA19469, NA12778, HG00246, HG00126, HG01075, NA12043, HG01148, HG00258, NA18632, NA19652, HG00155, HG00254, NA19390, NA19712, NA19434, NA19072, NA19444, NA19010, HG01357, NA20790, HG01375, NA19470, NA19311, HG01113, NA20544, HG00116, NA19783, HG00662, NA18615, HG01342, NA12347, HG00339, NA19785, NA19779, NA19716, NA19102, NA18873, HG00112, NA20758, NA19080, HG00377, NA20502, NA19129, HG01125, NA12006, NA12154, NA19074, NA18487, HG00553, HG01060, NA11830, NA19700, HG01098, HG01356, HG00231, HG00249, NA11995, NA19914, HG00187, NA19332, HG01079, HG00100, NA11933, NA18599, HG01389, HG01374, HG00318, HG01465, HG01456, NA12058, NA20808, HG00150, NA20507, NA18870, NA12400, NA12413, NA12341, NA19068, HG00251, HG00501, HG01488, NA20586, NA19723, NA11992, HG00346, NA12283, HG01354, NA20540, NA19313, NA12287, HG00247, HG00369, NA20513, NA19681, NA18964, NA19404, NA12761, NA12282, HG01455, HG01067, HG00106, HG01170, HG00236, HG01495, NA19471, HG01440, HG00309, HG00182, HG00427, NA19725, HG00159, HG00178, NA12748, NA11993, HG00464, NA11831, HG00313, HG00133, HG00149, HG01360, NA20524, HG01384, NA12003, HG00475, NA18516, NA19982, HG00320, NA18910, NA20770, HG01390, HG01073, HG00273, NA19449, NA19655, HG00373, HG01197, NA11894, NA18856, NA12249, HG00117, HG00157, NA18853, NA12827, HG00276, HG01204, NA20765, NA20801, HG00119, NA11881, NA18961, NA18543, NA12775, HG00366, HG01253, NA20804, NA07051, NA19334, HG01494, NA19786, NA19467, NA07037, NA19085, HG00269, HG00125, NA19248, NA12749, HG01055, HG00174, HG00123, NA12830, NA20807, NA19726, HG00343, NA20528, HG00372, HG01377, HG00472, HG01378, NA19755, HG00345, NA07000, HG00437, NA12776
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv456e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss266
Observed Complex0
Frequencyn/a


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