A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1049e199



Internal ID20124351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:151410172..151413398hg38UCSC Ensembl
chr5:150789733..150792959hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg383227
hg193227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2674159, esv2657079, esv2668403
SamplesNA19701, HG00542, NA19058, HG00143, NA19703, HG00608, NA18621, HG00671, NA19066, HG00559, NA18565, NA12843, NA11931, NA18999, NA20512, NA12751, NA19355, NA20332, NA18530, NA18959, HG00737, HG01461, HG00654, NA19443, HG01051, NA18633, NA19067, NA18602, NA18627, HG00337, NA19107, NA20814, NA07346, NA18563, NA18940, HG00122, NA18597, HG01177, HG01167, NA20774, HG01168, NA18547, NA18916, NA18574, NA11918, NA07347, NA19457, HG01083, HG00334, NA19384, HG00537, NA20291, NA19079, HG00512, HG00139, NA20539, HG01069, HG01080, HG00156, NA18868, NA11932, NA19372, NA11994, HG00534, NA19722, HG00118, NA18985, HG00326, NA20757, NA18867, NA19789, NA19921, NA20753, HG00137, HG00154, NA18605, HG00443, NA18538, HG01171, NA19056, NA19403, HG00557, HG00732, HG00657, NA20760, HG00583, HG00275, NA18572, HG00551, NA12234, HG00692, NA18548, NA18573, HG00651, HG00250, HG00690, HG00331, NA19453, NA18532, HG01497, NA19059, NA18555, HG00146, NA19452, NA18963, HG00704, NA19682, NA19395, NA18570, NA19625, NA18593, NA12546, HG01107, NA18541, NA12043, HG01148, NA18632, NA19652, NA19390, HG00265, NA19147, NA18564, NA18628, NA19072, HG01551, NA19331, NA19010, HG01357, NA19835, HG00473, NA19311, HG01137, NA19083, HG00662, HG00418, HG01489, HG00620, HG00614, HG00513, HG00478, HG00259, NA19779, NA19716, NA18636, NA18609, HG00280, NA11843, NA19780, NA18983, NA18989, HG01125, NA18624, NA19463, NA19063, NA19065, NA18612, NA19074, HG01516, HG00593, HG00626, HG00592, HG01356, NA20543, NA19055, HG00536, HG00231, NA19397, HG00249, NA18592, HG01359, HG00524, NA19914, HG00187, NA18561, NA19704, HG01188, NA18599, HG01389, HG00306, NA18545, NA19057, NA18596, NA12058, NA18606, HG00177, NA19190, NA12400, HG01140, NA12341, HG00327, NA19381, HG00501, NA19382, NA18489, NA19762, NA19728, HG00702, HG00689, HG00173, NA18982, NA19916, HG00330, HG00634, NA18942, HG00610, NA19088, HG00247, NA19138, NA19054, HG01110, HG00590, HG01455, HG00120, NA18977, NA18560, NA19731, NA19075, HG00422, NA19087, HG01440, NA19002, HG00427, NA19725, HG00178, NA18973, HG00530, HG00419, NA18638, HG00260, NA19007, NA18614, NA10847, HG00543, NA18544, HG00560, NA18613, HG00629, HG01360, HG00596, HG00328, NA19077, HG00701, NA19391, NA18991, HG00475, HG00436, NA18637, NA19788, NA20506, NA18630, HG00619, HG00708, HG01094, NA19000, HG01197, HG00613, HG00276, NA18536, NA18634, NA18945, NA18576, NA18546, NA18535, HG00285, NA19834, NA18559, HG00565, HG00366, NA18941, HG00278, NA19773, NA19380, NA19334, HG00256, HG00269, HG00125, NA19759, NA19078, HG00707, NA20582, NA19472, NA18987, HG00656, HG00698, HG00131, NA19726, NA18984, NA07056, HG01378, NA19755, NA18488, HG01082, NA18549, HG01191, NA18622, NA18965
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1049e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss296
Observed Complex0
Frequencyn/a


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