A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16961868



Internal ID41881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:15574883..15575277hg38UCSC Ensembl
chr5:15574992..15575386hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38395
hg19395
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5461384
Supporting Variants
Samples
Known GenesFBXL7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16961868
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001561


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