A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14347344



Internal ID22226365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:40566552..40611534hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3844983
Variant TypeCNV duplication
Copy Number40
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3218880
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14347344
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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