A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18233046



Internal ID20800086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:98511528..98512008hg38UCSC Ensembl
chr12:98905306..98905786hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg38481
hg19481
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6577660
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18233046
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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