A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225120



Internal ID20792160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:50190579..50190962hg38UCSC Ensembl
chr12:50584362..50584745hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg38384
hg19384
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581785
Supporting Variants
Samples
Known GenesLIMA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225120
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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