A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16962491



Internal ID42302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:3984488..4019659hg38UCSC Ensembl
chr5:3984602..4019773hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3835172
hg1935172
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5554362
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16962491
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000624


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