A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18256549



Internal ID20823589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:113787654..113789652hg38UCSC Ensembl
chr2:114545231..114547229hg19UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg381999
hg191999
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6545743
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18256549
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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