A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16269932



Internal ID20479150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:131311763..131646327hg38UCSC Ensembl
chr12:131796308..132130872hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg38334565
hg19334565
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4762884
Supporting Variants
Samples
Known GenesLOC338797
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16269932
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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