A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226811



Internal ID20793851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:76938418..76939880hg38UCSC Ensembl
chr13:77512552..77514015hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg381463
hg191464
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6594046
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226811
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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