A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18277360



Internal ID20844400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:16116242..16280654hg38UCSC Ensembl
chr8:15973751..16138163hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38164413
hg19164413
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6574678
Supporting Variants
Samples
Known GenesMSR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18277360
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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