A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17583951



Internal ID21775994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:89769348..89769654hg38UCSC Ensembl
chr9:92470795..92471101hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6014519
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17583951
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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