A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16965622



Internal ID44400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:54823657..54831229hg38UCSC Ensembl
chr5:54119485..54127057hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg387573
hg197573
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563514
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16965622
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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