A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16966617



Internal ID45065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:63579024..63600455hg38UCSC Ensembl
chr5:62874851..62896282hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg3821432
hg1921432
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5560924
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16966617
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000468


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