A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5516207



Internal ID292671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:39424461..39431291hg38UCSC Ensembl
chr20:38053104..38059934hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg386831
hg196831
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17732355
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5516207
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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