A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14346306



Internal ID22200835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:76304635..76307076hg38UCSC Ensembl
chr9:78919551..78921992hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg382442
hg192442
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3528889
Supporting Variants
SamplesHG00732
Known GenesPCSK5
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14346306
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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