A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17552831



Internal ID21877186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:69220530..69297066hg38UCSC Ensembl
chr4:70086248..70162784hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3876537
hg1976537
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6105916
Supporting Variants
Samples
Known GenesUGT2B28
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17552831
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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