A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18269421



Internal ID20836461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:157586774..157587526hg38UCSC Ensembl
chr5:157013782..157014534hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg38753
hg19753
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6555960
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18269421
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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