A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14346043



Internal ID22270014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:43006966..43019614hg38UCSC Ensembl
chr9:42963634..42976299hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3812649
hg1912666
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3213491
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14346043
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