A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5883828



Internal ID22658810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:37328626..37329180hg38UCSC Ensembl
chr2:37555769..37556323hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg38555
hg19555
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17390955
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5883828
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