A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5906956



Internal ID22682160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:43840729..43841273hg38UCSC Ensembl
chr3:43882221..43882765hg19UCSC Ensembl
Cytoband3p21.33
Allele length
AssemblyAllele length
hg38545
hg19545
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17421434
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5906956
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