A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14349630



Internal ID22206770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96157801..96157909hg38UCSC Ensembl
chr9:98920083..98920191hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV duplication
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3220244
Supporting Variants
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14349630
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