A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv390e199



Internal ID22758163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35135939..35147236hg38UCSC Ensembl
chr14:35605145..35616442hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg3811298
hg1911298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2672986, esv2658887, esv2671562, esv2664067
SamplesHG00442, NA19058, NA20529, HG01462, HG00608, NA18621, NA18947, NA20508, NA20816, NA18999, HG00181, NA18530, NA18959, NA18616, HG00449, HG01051, NA18602, HG01522, HG00693, NA18988, NA18627, HG00337, HG00663, NA18563, HG01350, HG00589, HG00272, HG01351, NA20774, NA18558, NA18547, NA18618, NA19062, NA18574, NA07048, NA18582, NA20768, NA18571, HG00311, NA11930, HG00281, HG00139, NA20539, NA20518, HG00335, NA20775, HG00232, HG00534, HG00705, NA19722, NA18990, NA18557, HG01048, HG00323, HG00253, NA20515, NA19789, NA18539, NA19921, HG01124, HG00154, NA18951, NA18605, NA20535, NA19908, HG00731, HG00443, HG00282, NA19070, HG00556, HG00263, HG01149, NA18948, NA18534, NA18981, HG00692, NA19064, NA18548, HG00740, NA18537, HG01102, NA18573, HG00651, HG00250, HG00404, HG00331, HG00684, NA18532, NA18553, NA19059, NA19761, NA18555, NA18963, HG00704, HG00463, NA12778, NA18570, NA18541, HG01075, NA19012, NA18974, NA18953, HG01148, NA19003, NA20799, HG00611, NA18632, HG00155, HG00254, NA19747, HG00353, NA18628, NA20815, NA19072, HG00580, HG00734, HG01357, NA20790, HG00473, HG00237, HG01137, NA19083, NA18943, NA20281, NA19783, HG00662, HG00418, NA18615, NA18610, HG01489, HG00620, HG00339, HG00614, HG00513, NA18631, NA19716, NA18609, HG00280, NA20758, NA19780, NA20503, HG00595, HG00628, NA18624, NA18623, NA18612, NA19074, HG01437, NA20772, HG01516, HG00593, HG00626, NA19648, NA11830, HG00592, HG01521, HG01356, NA19055, HG00536, HG00249, NA18592, HG01359, NA18980, NA20531, NA18599, HG00640, HG01465, HG00699, NA18545, NA19393, NA19057, NA18596, HG01456, NA20507, NA18526, HG01140, HG00327, HG01250, NA18550, HG01366, HG01070, NA19728, HG01488, NA20586, NA18635, HG00330, NA20769, HG00346, NA12283, HG01354, NA19088, NA19054, HG00270, NA19681, NA18964, HG00590, NA12282, NA19651, HG00262, NA19719, HG01072, NA18560, NA19731, NA19075, HG00422, NA18986, HG00309, NA19002, HG00159, NA19445, NA18975, NA20533, NA18973, HG00419, NA18638, HG00464, NA19007, HG01353, HG00543, HG01136, HG00560, HG00629, NA19657, NA19082, NA20524, HG00328, HG00428, NA20809, HG00577, HG00701, NA20536, HG00475, HG00436, HG00320, HG00584, NA18637, HG00500, NA20506, NA19658, NA18630, NA20344, HG00619, HG00708, HG00635, NA18566, HG01073, HG00273, NA19000, NA19655, HG00373, HG00117, HG00525, NA20828, NA20542, NA18634, NA18945, HG00476, NA19834, NA19108, NA18961, NA18952, NA18543, NA18950, NA18941, NA19773, NA07051, HG00607, NA19786, NA19085, HG00125, HG00707, HG00578, NA18971, HG00421, HG00329, HG00123, HG00698, NA18552, HG01251, NA18984, HG00472, NA19004, HG01097, HG00180, NA18622, HG00437, NA18562, NA18965, NA20509
Known GenesKIAA0391
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv390e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss289
Observed Complex0
Frequencyn/a


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