A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18263061



Internal ID20830101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:13189128..13189482hg38UCSC Ensembl
chr4:13190752..13191106hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg38355
hg19355
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6559411
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18263061
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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