A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17592635



Internal ID21784678
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 StatusS
Merged Variantsnsv6009951
Supporting Variants
Samples
Known GenesMOB3B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17592635
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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