A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5466221



Internal ID244066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:145806533..145806742hg38UCSC Ensembl
chr4:146727685..146727894hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38210
hg19210
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16956558
Samples
Known GenesZNF827
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5466221
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