A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5453899



Internal ID232009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:27597529..27611030hg38UCSC Ensembl
chr3:27639020..27652521hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3813502
hg1913502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16930345
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5453899
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