A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17555779



Internal ID21880134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:28596784..28596860hg38UCSC Ensembl
chr5:28596891..28596967hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5999799
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17555779
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