A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5895827



Internal ID22670914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:21762040..21770702hg38UCSC Ensembl
chr3:21803532..21812194hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg388663
hg198663
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17415062
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5895827
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