A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16958058



Internal ID39359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:149368742..149369001hg38UCSC Ensembl
chr4:150289894..150290153hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg38260
hg19260
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5557019
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16958058
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.026546


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