A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5846379



Internal ID22621314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:95315351..95322035hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg386685
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17503211
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5846379
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