A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18263450



Internal ID20830490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:106514089..106536339hg38UCSC Ensembl
chr4:107435246..107457496hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3822251
hg1922251
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6571026
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18263450
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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