A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5531025



Internal ID306989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:41395346..41395691hg38UCSC Ensembl
chr20:40023986..40024331hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg38346
hg19346
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17732401
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5531025
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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