A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18264482



Internal ID20831522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:174263854..174264413hg38UCSC Ensembl
chr4:175185005..175185564hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38560
hg19560
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6564603
Supporting Variants
Samples
Known GenesFBXO8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18264482
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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