A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18276397



Internal ID20843438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:108192613..108197244hg38UCSC Ensembl
chr8:109204842..109209473hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg384632
hg194632
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6572985
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18276397
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0017


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