A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17025193



Internal ID84525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:108209576..108211816hg38UCSC Ensembl
chr9:110971856..110974096hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg382241
hg192241
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5482799
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17025193
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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