A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16941894



Internal ID28618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:154997783..155063938hg38UCSC Ensembl
chr3:154715572..154781727hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3866156
hg1966156
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5554795
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16941894
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000937


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