A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231472



Internal ID20798512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:41236110..41237227hg38UCSC Ensembl
chr13:41810246..41811363hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg381118
hg191118
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6588357
Supporting Variants
Samples
Known GenesMTRF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231472
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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