A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862079



Internal ID22637014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87138519..87145835hg38UCSC Ensembl
chr9:89753434..89760750hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg387317
hg197317
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17514590
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862079
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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