A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16968487



Internal ID46306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:77733800..77744255hg38UCSC Ensembl
chr5:77029625..77040079hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg3810456
hg1910455
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5459404
Supporting Variants
Samples
Known GenesTBCA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16968487
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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