A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18279777



Internal ID20846817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:122176776..122177577hg38UCSC Ensembl
chr9:124939055..124939856hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38802
hg19802
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6570001
Supporting Variants
Samples
Known GenesMORN5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18279777
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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