A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874203



Internal ID22649154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35686809..35706611hg38UCSC Ensembl
chr20:34274731..34294533hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3819803
hg1919803
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17485341
Samples
Known GenesNFS1, RBM39, ROMO1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874203
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