A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17028097



Internal ID86428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129540978..129547572hg38UCSC Ensembl
chr9:132303257..132309851hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg386595
hg196595
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5487367
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17028097
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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