A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17016643



Internal ID78751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:104960294..105038067hg38UCSC Ensembl
chr8:105972522..106050295hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3877774
hg1977774
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6147407
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17016643
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.032011


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