A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18227817



Internal ID20794857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110030371..110031030hg38UCSC Ensembl
chr12:110468176..110468835hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38660
hg19660
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6575924
Supporting Variants
Samples
Known GenesANKRD13A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18227817
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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