A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5993778



Internal ID21903121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:62221153..62221226hg38UCSC Ensembl
chr3:62206827..62206900hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17550046
Samples
Known GenesPTPRG
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5993778
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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