A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865805



Internal ID22640740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:52783603..52789007hg38UCSC Ensembl
chr13:53357738..53363142hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg385405
hg195405
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17465637
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865805
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