A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5941125



Internal ID22716544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:13802015..13802080hg38UCSC Ensembl
chr16:13895872..13895937hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17387657
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5941125
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