A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5884391



Internal ID22659373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41765956..41767068hg38UCSC Ensembl
chr19:42269864..42270977hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg381113
hg191114
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17475963, nssv17475964
Samples
Known GenesCEACAM6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5884391
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