A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5977843



Internal ID22752778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:38157315..38290532hg38UCSC Ensembl
chr3:38198806..38332023hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38133218
hg19133218
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17425269
Samples
Known GenesOXSR1, SLC22A13
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5977843
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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