A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224933



Internal ID20791973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:85944867..85955733hg38UCSC Ensembl
chr12:86338646..86349512hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg3810867
hg1910867
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6593761
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224933
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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