A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5831598



Internal ID22606533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:138832219..138835246hg38UCSC Ensembl
chr2:139589789..139592816hg19UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg383028
hg193028
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17487682
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5831598
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