A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220080



Internal ID20787120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:112995421..113022645hg38UCSC Ensembl
chr13:113649735..113676959hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3827225
hg1927225
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6592308
Supporting Variants
Samples
Known GenesMCF2L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220080
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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