A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5999832



Internal ID21909175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:32552781..32552849hg38UCSC Ensembl
chr5:32552887..32552955hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17555760
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5999832
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