A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17705989



Internal ID129655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:55760563..55833130hg38UCSC Ensembl
chr16:55794475..55867042hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3872568
hg1972568
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563138
Supporting Variants
Samples
Known GenesCES1, CES1P1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17705989
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.225796


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