A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5515068



Internal ID291555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:4792272..4792435hg38UCSC Ensembl
chr20:4772918..4773081hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17730515
Samples
Known GenesRASSF2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5515068
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