A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14348435



Internal ID22205387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128395662..128395849hg38UCSC Ensembl
chr9:131157941..131158128hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38188
hg19188
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3213007
Supporting Variants
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14348435
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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