A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16272274



Internal ID20481492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21668332..21668332hg38UCSC Ensembl
chr14:22136546..22136546hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38174
hg19174
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4758385
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16272274
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