A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6001181



Internal ID21910524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:37544733..37544857hg38UCSC Ensembl
chr9:37544730..37544854hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17580719
Samples
Known GenesFBXO10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6001181
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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