A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16275905



Internal ID20485123
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 StatusS
Merged Variantsnsv4742384
Supporting Variants
Samples
Known GenesPRUNE2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16275905
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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