A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16980781



Internal ID54559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:22272387..22420977hg38UCSC Ensembl
chr6:22272616..22421206hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38148591
hg19148591
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5472727
Supporting Variants
Samples
Known GenesPRL
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16980781
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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