A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3219886



Internal ID22364760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109665951..109666011hg38UCSC Ensembl
chr13:110318298..110318358hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2436n152
Supporting Variantsnssv14368642, nssv14368643
SamplesNA19238, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3219886
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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