A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589221



Internal ID20962292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:63530035..63530593hg38UCSC Ensembl
chr15:63822234..63822792hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38559
hg19559
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238775
Samples
Known GenesUSP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589221
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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