A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18266463



Internal ID20833503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:10280833..10282528hg38UCSC Ensembl
chr5:10280945..10282640hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg381696
hg191696
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6568789
Supporting Variants
Samples
Known GenesCMBL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18266463
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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