A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5640866



Internal ID21589171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:122191048..122191048hg38UCSC Ensembl
chr9:124953327..124953327hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg383222
hg193222
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17159883
SamplesHG02587
Known GenesMORN5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5640866
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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