A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5832829



Internal ID22607764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:240266974..240271273hg38UCSC Ensembl
chr2:241206391..241210690hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg384300
hg194300
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17483434
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5832829
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