A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17577838



Internal ID21769881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:28524000..28631573hg38UCSC Ensembl
chr9:28523998..28631571hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38107574
hg19107574
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6007190
Supporting Variants
Samples
Known GenesLINGO2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17577838
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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