A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5626919



Internal ID21575224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:101551616..101551616hg38UCSC Ensembl
chr9:104313898..104313898hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17143779
SamplesHG00513
Known GenesRNF20
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5626919
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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