A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5447403



Internal ID225707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:72085361..72087842hg38UCSC Ensembl
chr3:72134512..72136993hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg382482
hg192482
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16934225
Samples
Known GenesLINC00877
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5447403
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