A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3206434



Internal ID22354975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:12132504..12162928hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3830425
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14302118, nssv14302124, nssv14302117, nssv14302120, nssv14302121, nssv14302119, nssv14302123, nssv14302122, nssv14302116
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3206434
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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