A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5888259



Internal ID22663262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9353884..9354088hg38UCSC Ensembl
chr3:9395568..9395772hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg38205
hg19205
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17428812
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5888259
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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