A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862036



Internal ID22636971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:20924700..20936968hg38UCSC Ensembl
chr9:20924699..20936967hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3812269
hg1912269
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17512213
Samples
Known GenesFOCAD
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862036
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