A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4750669



Internal ID20526590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:69220529..69383671hg38UCSC Ensembl
chr4:70086247..70249389hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38163143
hg19163143
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv59n199
Supporting Variantsnssv16292605
Samples
Known GenesUGT2B28
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4750669
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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