A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5860732



Internal ID22635667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:42944544..42949053hg38UCSC Ensembl
chr9:44022066..44026575hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg384510
hg194510
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2119n209
Supporting Variantsnssv17513524, nssv17513523
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5860732
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