A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226858



Internal ID20793898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:111477339..111477873hg38UCSC Ensembl
chr12:111915143..111915677hg19UCSC Ensembl
Cytoband12q24.12
Allele length
AssemblyAllele length
hg38535
hg19535
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6589399
Supporting Variants
Samples
Known GenesATXN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226858
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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