A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5626459



Internal ID21574764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97913251..97913251hg38UCSC Ensembl
chr9:100675533..100675533hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38427
hg19427
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17163424
SamplesHG00512
Known GenesC9orf156
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5626459
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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