A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5520666



Internal ID296985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41417746..41423703hg38UCSC Ensembl
chr19:41923651..41929608hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg385958
hg195958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17723499
Samples
Known GenesBCKDHA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5520666
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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