A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18279828



Internal ID20846868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:124374845..124375331hg38UCSC Ensembl
chr9:127137124..127137610hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38487
hg19487
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6557519
Supporting Variants
Samples
Known GenesPSMB7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18279828
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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