A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220416



Internal ID20787456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:131313962..131644193hg38UCSC Ensembl
chr12:131798507..132128738hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg38330232
hg19330232
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6589500
Supporting Variants
Samples
Known GenesLOC338797
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220416
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00848


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