A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17729463



Internal ID153129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:45176477..45177323hg38UCSC Ensembl
chr22:45572358..45573204hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg38847
hg19847
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5541795
Supporting Variants
Samples
Known GenesNUP50
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17729463
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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