A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5856545



Internal ID22631480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110041758..110047305hg38UCSC Ensembl
chr13:110694105..110699652hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg385548
hg195548
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17462055
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5856545
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