A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17541110



Internal ID21865465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:29616102..29695865hg38UCSC Ensembl
chr5:29616209..29695972hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3879764
hg1979764
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5999813
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17541110
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