A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18276366



Internal ID20843407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:106767961..106768696hg38UCSC Ensembl
chr8:107780189..107780924hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38736
hg19736
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6558965
Supporting Variants
Samples
Known GenesABRA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18276366
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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