A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16960871



Internal ID41225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:2097087..2097308hg38UCSC Ensembl
chr5:2097201..2097422hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38222
hg19222
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5455563
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16960871
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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