A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16977688



Internal ID52513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:177953324..177980500hg38UCSC Ensembl
chr5:177380325..177407501hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3827177
hg1927177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5465429
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16977688
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000158


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