A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5950390



Internal ID22725790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:98119801..98119801hg38UCSC Ensembl
chr9:100882083..100882083hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17447647
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5950390
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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