A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17560381



Internal ID21884736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:152972827..152972912hg38UCSC Ensembl
chr6:153293962..153294047hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6010075
Supporting Variants
Samples
Known GenesFBXO5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17560381
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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