A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5514157



Internal ID290658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:23689167..23751000hg38UCSC Ensembl
chr20:23669804..23731637hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3861834
hg1961834
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17731637
Samples
Known GenesCST1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5514157
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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