A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17556627



Internal ID21880982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:33514716..33514812hg38UCSC Ensembl
chr5:33514821..33514917hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5999450
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17556627
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