A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5909070



Internal ID22684280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:111944303..111944552hg38UCSC Ensembl
chr9:114706583..114706832hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38250
hg19250
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17435137
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5909070
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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