A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5898492



Internal ID22673608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:89027664..89035657hg38UCSC Ensembl
chr3:89076814..89084807hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg387994
hg197994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17417803
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5898492
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