A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766954



Internal ID20542814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:36173592..36173592hg38UCSC Ensembl
chr14:36642798..36642798hg19UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16281801
Samples
Known GenesPTCSC3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766954
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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