A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16973646



Internal ID49814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:110907408..110922452hg38UCSC Ensembl
chr5:110243107..110258151hg19UCSC Ensembl
Cytoband5q22.1
Allele length
AssemblyAllele length
hg3815045
hg1915045
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5560144
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16973646
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000468


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