A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17024367



Internal ID83981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:75144700..75144751hg38UCSC Ensembl
chr9:77759616..77759667hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5408887
Supporting Variants
Samples
Known GenesOSTF1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17024367
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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