A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6009951



Internal ID21919294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:27442549..27452522hg38UCSC Ensembl
chr9:27442547..27452520hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg389974
hg199974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17592635
Samples
Known GenesMOB3B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6009951
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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