A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4759907



Internal ID20535767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:123979106..123991039hg38UCSC Ensembl
chr9:126741385..126753318hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3811934
hg1911934
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv78n199
Supporting Variantsnssv16278936
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4759907
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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