A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17731466



Internal ID155132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:20351384..20351482hg38UCSC Ensembl
chr20:20332028..20332126hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5527812
Supporting Variants
Samples
Known GenesC20orf26
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17731466
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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