A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866917



Internal ID22641852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:7854447..7866376hg38UCSC Ensembl
chr9:7854447..7866376hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3811930
hg1911930
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17514362
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866917
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