A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18276237



Internal ID20843278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:128891466..128891661hg38UCSC Ensembl
chr8:129903712..129903907hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg38196
hg19196
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6559898
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18276237
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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