A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843768



Internal ID22618703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:137363976..137369072hg38UCSC Ensembl
chr6:137685113..137690209hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg385097
hg195097
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17501758
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843768
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