A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5832862



Internal ID22607797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:32068247..32074146hg38UCSC Ensembl
chr2:32293316..32299215hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg385900
hg195900
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17484128, nssv17484127
Samples
Known GenesSPAST
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5832862
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer