A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17025339



Internal ID84625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:82768234..82787201hg38UCSC Ensembl
chr9:85383149..85402116hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3818968
hg1918968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5486229
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17025339
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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