A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3220897



Internal ID22365457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:10940790..10945005hg38UCSC Ensembl
chrUn_gl000241:16218..20433hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg384216
hg194216
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14302628, nssv14302633, nssv14302635, nssv14302634, nssv14302627, nssv14302631, nssv14302629, nssv14302630, nssv14302632
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)nsv3220897
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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