A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18230502



Internal ID20797542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:93452369..93453397hg38UCSC Ensembl
chr12:93846145..93847173hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg381029
hg191029
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6590983
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18230502
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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