A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4749601



Internal ID20525633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:171931801..171931868hg38UCSC Ensembl
chr5:171358805..171358872hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16259920
Samples
Known GenesFBXW11
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4749601
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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