A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223682



Internal ID20790722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:118046308..118046782hg38UCSC Ensembl
chr12:118484113..118484587hg19UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg38475
hg19475
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6580031
Supporting Variants
Samples
Known GenesWSB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223682
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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