A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv833e199



Internal ID20124135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38960540..38993337hg38UCSC Ensembl
chr22:39356545..39389342hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3832798
hg1932798
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2661117, esv2670643, esv2675350, esv2663727, esv2660577, esv2666691
SamplesHG01441, HG00650, HG00542, NA19055, HG01462, HG00608, NA18947, NA19664, HG00671, NA19066, HG00559, HG00187, NA18561, HG01389, HG01374, HG00306, NA18999, NA18603, HG00181, HG00699, NA18545, NA19057, HG01456, HG00566, NA18959, HG00177, NA18526, NA18602, NA18988, NA18627, HG00327, NA19660, NA18944, HG01366, HG00589, HG00272, HG00501, NA19448, NA18595, NA19678, HG01492, HG00634, NA18960, NA18618, HG00736, NA19088, NA18571, NA19054, HG00334, NA19782, HG00590, NA18611, HG01134, HG00512, HG00277, HG01455, HG00325, NA19719, HG01072, NA18560, NA19731, HG00422, NA18986, HG01440, NA19722, HG00427, HG00118, NA18990, NA18985, HG00323, NA18973, HG00530, HG00419, NA19789, HG00464, NA19007, NA18614, HG00543, HG00313, HG00188, NA18951, NA18544, HG00560, NA18605, NA18613, HG00629, HG00443, HG01360, NA19082, HG01187, HG01171, NA19056, HG00557, HG00328, NA19077, HG00428, HG00653, NA18956, HG00701, HG00657, NA19717, HG00556, HG00320, HG00533, NA19081, HG00500, NA18579, NA18572, NA18976, NA18948, NA19776, HG00708, HG00635, NA19064, NA18537, HG01390, NA18566, HG01073, HG00651, NA19774, NA19655, HG00690, HG00404, HG00531, HG00684, NA19750, NA18532, HG01101, HG00525, NA19059, HG00276, HG00704, HG00463, NA18634, NA18945, NA19012, NA18608, NA19685, NA19003, NA18632, NA19652, NA18542, NA18535, NA18961, NA18952, NA18543, NA18559, HG00625, NA19749, NA18628, NA19072, NA18950, HG00580, NA19732, HG00734, NA07051, HG01375, HG00473, NA19786, HG01137, NA18943, HG00418, NA19085, NA19759, HG00707, HG00672, HG00614, HG00478, NA18971, NA18631, NA19060, HG00421, NA18987, HG00656, HG01254, NA18636, HG00310, NA19770, HG00698, NA19726, HG01251, NA19661, HG01377, NA18984, HG00472, NA19004, NA18624, NA18623, NA19065, HG01191, NA18622, HG00437, NA18562, NA18620, HG00593
Known GenesAPOBEC3A, APOBEC3A_B, APOBEC3B, APOBEC3B-AS1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv833e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss195
Observed Complex0
Frequencyn/a


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