A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268660



Internal ID20835700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:148387692..148390048hg38UCSC Ensembl
chr5:147767255..147769611hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg382357
hg192357
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6568209
Supporting Variants
Samples
Known GenesFBXO38
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268660
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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