A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18264852



Internal ID20831892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15634367..15635179hg38UCSC Ensembl
chr4:15635990..15636802hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg38813
hg19813
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6563709
Supporting Variants
Samples
Known GenesFBXL5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18264852
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00017


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