A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3211592



Internal ID22359104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38962064..38992000hg38UCSC Ensembl
chr22:39358069..39388005hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3829937
hg1929937
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14303568, nssv14303570, nssv14303569
SamplesHG00512, HG00513, HG00514
Known GenesAPOBEC3A, APOBEC3A_B, APOBEC3B, APOBEC3B-AS1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3211592
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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