A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17541404



Internal ID21865759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:68809408..69220530hg38UCSC Ensembl
chr4:69675126..70086248hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38411123
hg19411123
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6112501
Supporting Variants
Samples
Known GenesUGT2A3, UGT2B10, UGT2B11, UGT2B7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17541404
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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