A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841556



Internal ID22616491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:16455811..16458476hg38UCSC Ensembl
chr5:16455920..16458585hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg382666
hg192666
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17497052
Samples
Known GenesZNF622
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841556
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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