A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4742384



Internal ID20518366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:76791225..76791371hg38UCSC Ensembl
chr9:79406141..79406287hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg38147
hg19147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16275905
Samples
Known GenesPRUNE2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4742384
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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