A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4012871



Internal ID22074502
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 Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155793
Supporting Variants
Samples
Known GenesAPOBEC3A, APOBEC3A_B, APOBEC3B, APOBEC3B-AS1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4012871
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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