A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6012524



Internal ID21921867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:107326310..107326375hg38UCSC Ensembl
chr9:110088591..110088656hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17593612
Samples
Known GenesRAD23B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6012524
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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