A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3528889



Internal ID22398282
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9605n152
Supporting Variantsnssv14346306
SamplesHG00732
Known GenesPCSK5
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3528889
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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