A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155793



Internal ID22086298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:38967614..38979302hg38UCSC Ensembl
Outerchr22:38955461..38993623hg38UCSC Ensembl
Innerchr22:39363619..39375307hg19UCSC Ensembl
Outerchr22:39351466..39389628hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3838163
hg1938163
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4012903, nssv4012858, nssv4012885, nssv4012893, nssv4012867, nssv4012878, nssv4012890, nssv4012870, nssv4012868, nssv4012865, nssv4012898, nssv4012891, nssv4012886, nssv4012902, nssv4012897, nssv4012879, nssv4012882, nssv4012889, nssv4012901, nssv4012856, nssv4012864, nssv4012881, nssv4012883, nssv4012871, nssv4012869, nssv4012887, nssv4012861, nssv4012874, nssv4012900, nssv4012873, nssv4012880, nssv4012863, nssv4012894, nssv4012875, nssv4012892, nssv4012857, nssv4012884, nssv4012859, nssv4012896, nssv4012876, nssv4012860, nssv4012862, nssv4012872, nssv4012895
Samples
Known GenesAPOBEC3A, APOBEC3A_B, APOBEC3B, APOBEC3B-AS1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155793
Frequency
Sample Size131
Observed Gain0
Observed Loss44
Observed Complex0
Frequencyn/a


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