A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229961



Internal ID20797001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:112080214..112080711hg38UCSC Ensembl
chr12:112518018..112518515hg19UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg38498
hg19498
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6592772
Supporting Variants
Samples
Known GenesNAA25
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229961
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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