A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17602819



Internal ID21794866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103155456..103155546hg38UCSC Ensembl
chr14:103621793..103621883hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6021516
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17602819
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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