A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5930825



Internal ID22706098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58489033..58491066hg38UCSC Ensembl
chr16:58522937..58524970hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg382034
hg192034
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17372515
Samples
Known GenesNDRG4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5930825
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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