A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5558160



Internal ID331232
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 StatusM
Merged Variants
Supporting Variantsnssv16955611
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5558160
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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