A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5601755



Internal ID21550405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:76304530..76306923hg38UCSC Ensembl
chr9:78919446..78921839hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg382394
hg192394
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17162999
SamplesHG00731
Known GenesPCSK5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5601755
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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