A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6064082



Internal ID21973315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:171866552..171866552hg38UCSC Ensembl
chr5:171293556..171293556hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17565088
Samples
Known GenesFBXW11
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6064082
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer