A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5904878



Internal ID22680057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:24308346..24313458hg38UCSC Ensembl
chr5:24308455..24313567hg19UCSC Ensembl
Cytoband5p14.2
Allele length
AssemblyAllele length
hg385113
hg195113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17413527
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5904878
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