A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865085



Internal ID22640020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:48572956..48583567hg38UCSC Ensembl
chr14:49042159..49052770hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3810612
hg1910612
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463698
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865085
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