A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220984



Internal ID20788024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:98560850..98561921hg38UCSC Ensembl
chr12:98954628..98955699hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg381072
hg191072
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6585082
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220984
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0006


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