A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6011097



Internal ID21920440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:107321243..107321296hg38UCSC Ensembl
chr9:110083524..110083577hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17593304
Samples
Known GenesRAD23B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6011097
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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