A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236298



Internal ID20803338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:98775737..98776917hg38UCSC Ensembl
chr12:99169515..99170695hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg381181
hg191181
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6579767
Supporting Variants
Samples
Known GenesANKS1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236298
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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