A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859430



Internal ID22634365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:43125020..43132619hg38UCSC Ensembl
chr8:42980163..42987762hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg387600
hg197600
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17509225, nssv17506671
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859430
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