A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5643273



Internal ID21591578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133105836..133105836hg38UCSC Ensembl
chr9:135981223..135981223hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17159797
SamplesHG03125
Known GenesRALGDS
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5643273
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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