A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5919459



Internal ID22694681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:109327613..109328259hg38UCSC Ensembl
chr9:112089893..112090539hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38647
hg19647
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17430994
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5919459
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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