A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17013101



Internal ID76406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:74175660..74183142hg38UCSC Ensembl
chr8:75087895..75095377hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg387483
hg197483
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5557430
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17013101
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.011396


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