A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5889336



Internal ID22664353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:20609245..20668802hg38UCSC Ensembl
chr3:20650737..20710294hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3859558
hg1959558
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17415179
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5889336
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