A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560982



Internal ID333971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:85719378..85761068hg38UCSC Ensembl
chr9:88334293..88375983hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3841691
hg1941691
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17024631
Samples
Known GenesAGTPBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560982
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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