A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5665110



Internal ID21613415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:62879129..62935061hg38UCSC Ensembl
chr9:66534953..66590885hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3855933
hg1955933
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17162579
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5665110
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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