A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17025357



Internal ID84639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:83066098..83068553hg38UCSC Ensembl
chr9:85681013..85683468hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg382456
hg192456
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5480963
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17025357
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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