A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843705



Internal ID22618640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110561396..110562695hg38UCSC Ensembl
chr6:110882599..110883898hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17500918
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843705
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