A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17022071



Internal ID82378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:28588206..28762059hg38UCSC Ensembl
chr9:28588204..28762057hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38173854
hg19173854
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5480938
Supporting Variants
Samples
Known GenesLINGO2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17022071
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000937


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