A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871204



Internal ID22646141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:45643502..45644667hg38UCSC Ensembl
chr21:47063416..47064581hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg381166
hg191166
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17488935, nssv17488936
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871204
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