A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6024893



Internal ID21934236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39248300..39254535hg38UCSC Ensembl
chr17:37404553..37410788hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg386236
hg196236
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17623114
Samples
Known GenesFBXL20
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6024893
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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