A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861921



Internal ID22636856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:107783169..107785893hg38UCSC Ensembl
chr9:110545450..110548174hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg382725
hg192725
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17510657
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5861921
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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