A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219791



Internal ID20786831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:75576345..75577051hg38UCSC Ensembl
chr13:76150481..76151187hg19UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg38707
hg19707
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576070
Supporting Variants
Samples
Known GenesUCHL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219791
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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