A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866218



Internal ID22641153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:89760612..89768970hg38UCSC Ensembl
chr9:92462059..92470417hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg388359
hg198359
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17514725
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866218
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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