A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6086110



Internal ID21995343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135901621..135901621hg38UCSC Ensembl
chr9:138793467..138793467hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg382475
hg192475
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17581294
Samples
Known GenesCAMSAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6086110
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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