A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859777



Internal ID22634712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90258189..90271002hg38UCSC Ensembl
chr9:93020471..93033284hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3812814
hg1912814
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17514730
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859777
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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