A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16955611



Internal ID37714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:110239213..110259812hg38UCSC Ensembl
chr4:111160369..111180968hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3820600
hg1920600
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5558160
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16955611
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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