A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562728



Internal ID20935799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:37552679..37553108hg38UCSC Ensembl
chr9:37552676..37553105hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg38430
hg19430
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18280678
Samples
Known GenesFBXO10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562728
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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