A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16977778



Internal ID52577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:180415324..180420862hg38UCSC Ensembl
chr5:179842324..179847862hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg385539
hg195539
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5467181
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16977778
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.024952


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