A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16975023



Internal ID50736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:132413708..132442214hg38UCSC Ensembl
chr5:131749400..131777906hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3828507
hg1928507
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5554412
Supporting Variants
Samples
Known GenesC5orf56
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16975023
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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