A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17027863



Internal ID86273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:117709024..117711116hg38UCSC Ensembl
chr9:120471302..120473394hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg382093
hg192093
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5478855
Supporting Variants
Samples
Known GenesTLR4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17027863
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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