A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16925420



Internal ID17694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:147018296..147018362hg38UCSC Ensembl
chr2:147775864..147775930hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563181
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16925420
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000781


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