A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18276417



Internal ID20843458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:109545174..109545670hg38UCSC Ensembl
chr8:110557403..110557899hg19UCSC Ensembl
Cytoband8q23.2
Allele length
AssemblyAllele length
hg38497
hg19497
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6570439
Supporting Variants
Samples
Known GenesEBAG9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18276417
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00058


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