A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17024908



Internal ID84326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:60522797..60527344hg38UCSC Ensembl
chr9_gl000199_random:4239..8786hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg384548
hg194548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5478093
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17024908
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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