A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226100



Internal ID20793140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:45482672..45483420hg38UCSC Ensembl
chr12:45876455..45877203hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg38749
hg19749
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581758
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226100
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00012


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