A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17011095



Internal ID75043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:28602362..28602437hg38UCSC Ensembl
chr8:28459879..28459954hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6147354
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17011095
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.021237


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