A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18266903



Internal ID20833943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:21154399..21155794hg38UCSC Ensembl
chr5:21154508..21155903hg19UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg381396
hg191396
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6571538
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18266903
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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