A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5854522



Internal ID22629457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:55226376..55227375hg38UCSC Ensembl
chr14:55693094..55694093hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17451272, nssv17460907
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5854522
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