A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568839



Internal ID20941910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:33827547..33828929hg38UCSC Ensembl
chr9:33827545..33828927hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg381383
hg191383
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18280518
Samples
Known GenesUBE2R2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568839
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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