A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5945576



Internal ID22721055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55387084..55387726hg38UCSC Ensembl
chr19:55898452..55899094hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38643
hg19643
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17409168
Samples
Known GenesRPL28
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5945576
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