A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6082228



Internal ID21991461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:27517503..27517503hg38UCSC Ensembl
chr9:27517501..27517501hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17586694
Samples
Known GenesMOB3B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6082228
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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