A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16259905



Internal ID20469123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:68552660..68552990hg38UCSC Ensembl
chr17:66548801..66549131hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4738288
Supporting Variants
Samples
Known GenesFAM20A
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16259905
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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