A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5552740



Internal ID326057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:10321549..10321560hg38UCSC Ensembl
chr20:10302197..10302208hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg38198
hg19198
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17730825
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5552740
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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