A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4745891



Internal ID20521902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57218716..57219039hg38UCSC Ensembl
chr16:57252628..57252951hg19UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16260194
Samples
Known GenesRSPRY1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4745891
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