A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5914418



Internal ID22689635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:27350439..27357560hg38UCSC Ensembl
chr9:27350437..27357558hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg387122
hg197122
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17439204
Samples
Known GenesMOB3B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5914418
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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