A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4751877



Internal ID20527737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:38157314..38290532hg38UCSC Ensembl
chr3:38198805..38332023hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38133219
hg19133219
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16283296
Samples
Known GenesOXSR1, SLC22A13
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4751877
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer