A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5638171



Internal ID21586476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:107388993..107388993hg38UCSC Ensembl
chr9:110151274..110151274hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17158143
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5638171
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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