A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5515910



Internal ID292383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:12441241..12486984hg38UCSC Ensembl
chr20:12421889..12467632hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3845744
hg1945744
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17730921
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5515910
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer