A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16893021



Internal ID169505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:181092758..181093573hg38UCSC Ensembl
chr1:181061894..181062709hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg38816
hg19816
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5554154
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16893021
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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