A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4757332



Internal ID20533192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:69220530..69380847hg38UCSC Ensembl
chr4:70086248..70246565hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38160318
hg19160318
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv59n199
Supporting Variantsnssv16279154
Samples
Known GenesUGT2B28
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4757332
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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