A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5860091



Internal ID22635026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:19706781..19708982hg38UCSC Ensembl
chr9:19706779..19708980hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg382202
hg192202
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17512167
Samples
Known GenesSLC24A2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5860091
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