A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226308



Internal ID20793348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:98476932..98479534hg38UCSC Ensembl
chr12:98870710..98873312hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg382603
hg192603
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576702
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226308
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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