A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569330



Internal ID20942401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128529802..128530904hg38UCSC Ensembl
chr9:131292081..131293183hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg381103
hg191103
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279981
Samples
Known GenesGLE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569330
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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