A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5919337



Internal ID22694559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:124806871..124807186hg38UCSC Ensembl
chr9:127569150..127569465hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17432033
Samples
Known GenesOLFML2A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5919337
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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