A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16935398



Internal ID24316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:109508455..109527242hg38UCSC Ensembl
chr3:109227302..109246089hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg3818788
hg1918788
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6147031
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16935398
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.004528


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