A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv179e199



Internal ID22757952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:133111161..133111939hg38UCSC Ensembl
chr10:134924665..134925443hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38779
hg19779
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2661218, esv2666117
SamplesNA19701, HG00650, NA19703, HG00608, NA19909, HG00142, NA19399, NA18565, NA11920, NA19359, NA19377, NA18530, NA18616, HG01461, HG00654, NA19443, NA18633, NA18602, HG00693, NA18988, NA18627, HG00337, HG00271, HG00663, HG00138, NA18597, HG01351, NA18960, NA19457, HG00334, HG00311, NA19130, NA19079, HG00512, HG00281, HG01069, NA20775, NA19372, HG00534, NA19172, HG00160, NA18990, HG01048, HG00326, HG00154, NA18605, HG00731, HG00443, NA18538, HG01171, HG00282, NA19056, HG00557, HG00732, HG00657, NA20760, NA19717, NA19455, NA20314, NA19663, HG00583, NA18579, NA18534, HG01047, NA18573, NA19084, HG00531, HG00479, NA12829, HG00331, HG00684, HG01101, HG00140, NA19009, NA18555, NA19452, NA18523, HG00463, NA19318, HG00126, NA19625, HG01107, NA18953, NA19003, NA20799, HG00625, NA18628, HG01357, NA19083, NA19360, HG00662, HG00418, NA18615, NA18610, HG01342, HG00620, HG00614, NA19785, NA19223, HG00342, NA19468, NA18636, NA18609, NA19116, HG00377, NA19430, NA19463, NA12154, NA18612, NA19429, NA19074, HG00553, HG00581, HG00626, HG01060, NA19700, NA19055, NA19397, HG01359, HG00524, HG01052, NA18980, NA18561, HG01188, NA18599, HG01389, HG01374, HG00318, NA18486, HG00699, NA18545, NA19819, NA18596, NA12058, NA18606, NA19190, NA19746, NA19396, NA19076, HG00501, NA19448, NA18595, HG01488, HG00702, HG00689, HG00448, HG00173, NA18635, NA19198, NA12348, HG00634, HG01354, NA19313, NA19088, HG00247, HG00369, NA19681, HG00590, NA18611, NA19404, HG01134, HG00277, NA19383, HG00106, HG01170, HG00236, NA18977, NA19719, HG01072, NA18560, NA19075, HG00422, NA19471, NA19087, HG00309, HG00427, HG00159, NA19445, HG00530, HG00419, HG00464, NA19007, NA18614, HG01353, HG00543, HG00313, HG01183, HG01136, HG00149, NA18544, NA18613, HG00629, NA19657, HG00183, NA18934, HG00596, HG00328, HG00428, HG00653, HG00577, HG00701, HG00584, HG00533, NA18637, HG00500, NA18910, HG00619, HG00708, NA18566, NA19774, HG00613, NA19436, NA18546, NA19401, HG00124, NA20773, NA18542, HG00285, NA19834, NA18961, NA18543, NA18559, NA19749, NA18950, HG00638, HG00278, NA19380, HG00607, NA19439, NA19786, NA19467, HG01108, HG00256, HG00125, NA19818, HG00672, HG00111, HG00578, HG01491, NA19060, HG00421, HG00656, HG01055, HG00123, HG00698, NA19213, HG01251, NA18984, NA19004, HG01082, NA18549, HG00180, HG00437, NA18562
Known GenesGPR123
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv179e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss254
Observed Complex0
Frequencyn/a


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