A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223228



Internal ID20790268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:44892688..44893261hg38UCSC Ensembl
chr13:45466823..45467396hg19UCSC Ensembl
Cytoband13q14.12
Allele length
AssemblyAllele length
hg38574
hg19574
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6579009
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223228
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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