A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17025190



Internal ID84523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:108131559..108131610hg38UCSC Ensembl
chr9:110893839..110893890hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5395234
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17025190
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001876


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