A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16267088



Internal ID20476306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75206200..75222750hg38UCSC Ensembl
chr16:75240098..75256648hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3816551
hg1916551
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4752738
Supporting Variants
Samples
Known GenesCTRB1, CTRB2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16267088
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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