A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1366e199



Internal ID20124668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104833861..104835106hg38UCSC Ensembl
chr9:107596142..107597387hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg381246
hg191246
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2660468, esv2675308
SamplesHG00626, NA12383, HG00189, HG00650, HG00542, NA19700, HG00592, HG01521, HG00536, HG00608, NA18621, NA18947, HG00671, NA18592, NA12414, NA18561, NA19704, HG01066, NA18999, NA20802, NA20512, NA18603, NA19819, NA19777, NA12340, NA18530, NA18606, NA18616, HG01051, NA18633, NA18602, HG00693, NA18627, HG00663, NA18563, NA19660, NA19076, NA19005, NA18597, HG00702, NA19723, NA18635, NA18567, NA19916, HG01492, HG00634, NA18942, HG00736, NA11918, NA07347, HG00346, NA18582, NA20768, NA19054, NA18498, NA20336, HG00537, NA20541, NA18611, HG00281, NA20539, NA19651, HG00120, HG00683, NA06984, NA20812, NA18560, NA19075, NA18617, HG00422, HG00705, NA18986, NA19087, HG01440, HG00309, NA19722, NA19002, NA18990, NA20342, NA18973, HG00253, NA20755, NA18638, HG00464, NA20818, NA18614, HG00543, HG00149, NA18544, NA18605, HG00443, NA19082, NA19056, NA19670, NA20524, HG00557, NA19077, HG00428, HG00732, HG00577, HG00657, NA19391, HG00475, NA19717, NA19236, HG00436, HG00584, HG00533, HG00583, NA19081, HG00500, HG00275, NA20506, NA18871, NA18948, NA18534, NA18630, HG00692, NA19064, NA19654, NA18566, HG00651, NA19000, HG00250, NA19655, NA18626, HG00404, HG00531, NA20581, HG01197, NA18532, NA06989, NA18963, HG00704, NA19756, NA18570, NA18945, NA18541, NA19012, NA18576, NA18608, NA19685, NA19003, HG00258, HG00611, NA18632, HG00476, NA18542, NA18535, NA11881, NA18543, NA18559, NA19712, NA18564, NA19747, HG00565, HG00366, NA18628, HG01551, HG00734, NA18941, NA20785, NA20527, HG01375, HG00473, HG00607, NA19679, NA19467, HG01137, HG00256, HG00662, HG00418, NA18615, HG01342, NA06986, HG00620, NA19818, NA19078, HG00707, HG00672, HG00513, NA18631, NA19223, NA19060, NA18987, NA12749, HG00656, NA19716, HG00267, HG00123, HG00698, NA20826, HG00343, NA20528, NA18552, NA18983, HG01251, HG00595, HG01464, NA19129, HG01111, NA18968, NA18624, NA19463, NA18522, HG01097, NA18549, NA20754, NA19074, NA18622, HG00437, NA18577
Known GenesABCA1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1366e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss212
Observed Complex0
Frequencyn/a


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