A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236278



Internal ID20803318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:40356797..40870008hg38UCSC Ensembl
chr13:40930934..41444144hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38513212
hg19513211
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6591837
Supporting Variants
Samples
Known GenesFOXO1, LINC00598, MIR320D1, MIR621, MRPS31, SLC25A15, TPTE2P5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236278
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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