A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3216643



Internal ID22362575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:107962806..107962910hg38UCSC Ensembl
chr9:110725087..110725191hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14348296, nssv14348297
SamplesNA19238, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3216643
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