A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6102270



Internal ID22011506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:31923288..31944045hg38UCSC Ensembl
chr9:31923286..31944043hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3820758
hg1920758
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17591696
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6102270
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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