A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6016061



Internal ID21925404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86206494..86228811hg38UCSC Ensembl
chr9:88821409..88843726hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3822318
hg1922318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17582721
Samples
Known GenesC9orf153
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6016061
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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