A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18266168



Internal ID20833208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:119084215..119084593hg38UCSC Ensembl
chr5:118419910..118420288hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38379
hg19379
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6574551
Supporting Variants
Samples
Known GenesDMXL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18266168
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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