A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18267133



Internal ID20834173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:109396003..109396116hg38UCSC Ensembl
chr5:108731704..108731817hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6570856
Supporting Variants
Samples
Known GenesPJA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18267133
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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