A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155322



Internal ID22085827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:55762477..55788532hg38UCSC Ensembl
Outerchr16:55761302..55795645hg38UCSC Ensembl
Innerchr16:55796389..55822444hg19UCSC Ensembl
Outerchr16:55795214..55829557hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3834344
hg1934344
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv118n97
Supporting Variantsnssv4008729, nssv4008674, nssv4008665, nssv4008678, nssv4008700, nssv4008684, nssv4008706, nssv4008711, nssv4008661, nssv4008695, nssv4008663, nssv4008699, nssv4008721, nssv4008703, nssv4008738, nssv4008681, nssv4008733, nssv4008717, nssv4008685, nssv4008742, nssv4008659, nssv4008676, nssv4008724, nssv4008704, nssv4008725, nssv4008689, nssv4008732, nssv4008693, nssv4008694, nssv4008662, nssv4008670, nssv4008712, nssv4008716, nssv4008709, nssv4008705, nssv4008715, nssv4008701, nssv4008683, nssv4008673, nssv4008713, nssv4008710, nssv4008696, nssv4008727, nssv4008739, nssv4008726, nssv4008698, nssv4008722, nssv4008687, nssv4008723, nssv4008688, nssv4008728, nssv4008736, nssv4008680, nssv4008679, nssv4008666, nssv4008660, nssv4008737, nssv4008707, nssv4008718, nssv4008714, nssv4008692, nssv4008690, nssv4008671, nssv4008668, nssv4008691, nssv4008740, nssv4008734, nssv4008677, nssv4008731, nssv4008682, nssv4008672, nssv4008669, nssv4008735, nssv4008720, nssv4008743, nssv4008667, nssv4008702
Samples
Known GenesCES1P1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155322
Frequency
Sample Size131
Observed Gain0
Observed Loss77
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer