A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5905833



Internal ID22681026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:157701927..157704281hg38UCSC Ensembl
chr3:157419716..157422070hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg382355
hg192355
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17417542
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5905833
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