A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17731464



Internal ID155130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:20333140..20338086hg38UCSC Ensembl
chr20:20313784..20318730hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg384947
hg194947
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5533670
Supporting Variants
Samples
Known GenesC20orf26
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17731464
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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