A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6016282



Internal ID21925625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113285342..113285393hg38UCSC Ensembl
chr9:116047622..116047673hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17580790
Samples
Known GenesPRPF4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6016282
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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