A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18276241



Internal ID20843282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:129123179..129124296hg38UCSC Ensembl
chr8:130135425..130136542hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg381118
hg191118
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6573938
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18276241
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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