A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5882809



Internal ID22657786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:12626527..12631965hg38UCSC Ensembl
chr2:12766653..12772091hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg385439
hg195439
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17392821
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5882809
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