A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16893105



Internal ID169558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:183148960..183150087hg38UCSC Ensembl
chr1:183118095..183119222hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg381128
hg191128
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5561119
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16893105
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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