A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17018555



Internal ID80012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:123465605..123467700hg38UCSC Ensembl
chr8:124477845..124479940hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg382096
hg192096
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5561334
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17018555
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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