A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17583586



Internal ID21775629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:32520809..32520868hg38UCSC Ensembl
chr9:32520807..32520866hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6008902
Supporting Variants
Samples
Known GenesDDX58
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17583586
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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