A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218962



Internal ID20786002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:117336879..117338251hg38UCSC Ensembl
chr12:117774684..117776056hg19UCSC Ensembl
Cytoband12q24.22
Allele length
AssemblyAllele length
hg381373
hg191373
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581581
Supporting Variants
Samples
Known GenesNOS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218962
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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