A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16282072



Internal ID20491290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:104764080..104764080hg38UCSC Ensembl
chr14:105230417..105230417hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4751064
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16282072
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