A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5878552



Internal ID22653518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:17764207..17785375hg38UCSC Ensembl
chr21:19136524..19157692hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3821169
hg1921169
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17480199
Samples
Known GenesC21orf91-OT1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5878552
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