A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5860258



Internal ID22635193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:94295482..94297614hg38UCSC Ensembl
chr14:94761819..94763951hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg382133
hg192133
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17469800
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5860258
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