A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5945047



Internal ID22720520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:86930024..86944764hg38UCSC Ensembl
chr14:87396368..87411108hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3814741
hg1914741
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17386750
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5945047
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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