A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5558831



Internal ID331884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91069561..91079805hg38UCSC Ensembl
chr9:93831843..93842087hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3810245
hg1910245
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17024975
Samples
Known GenesLOC100129316
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5558831
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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