A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5633247



Internal ID21581552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:78089951..78089951hg38UCSC Ensembl
chr9:80704867..80704867hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17162852
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5633247
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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