A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16974727



Internal ID50528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:149108300..149109137hg38UCSC Ensembl
chr5:148487863..148488700hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38838
hg19838
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5554341
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16974727
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000468


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