A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229281



Internal ID20796321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:20881275..20881849hg38UCSC Ensembl
chr13:21455414..21455988hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38575
hg19575
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6585449
Supporting Variants
Samples
Known GenesXPO4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229281
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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