A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5856518



Internal ID22631453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:72133921..72135080hg38UCSC Ensembl
chr13:72708059..72709218hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg381160
hg191160
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17469363
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5856518
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