A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17731863



Internal ID155529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:30976835..30980911hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg384077
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5516918
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17731863
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.002344


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