A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16975567



Internal ID51102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:145691453..145692233hg38UCSC Ensembl
chr5:145071016..145071796hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38781
hg19781
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5560717
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16975567
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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