A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226262



Internal ID20793302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:131312886..131645267hg38UCSC Ensembl
chr12:131797431..132129812hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg38332382
hg19332382
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6582872
Supporting Variants
Samples
Known GenesLOC338797
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226262
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.08528


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