A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220992



Internal ID20788032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:125083830..125084259hg38UCSC Ensembl
chr12:125568376..125568805hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38430
hg19430
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6587406
Supporting Variants
Samples
Known GenesAACS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220992
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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