A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5640702



Internal ID21589007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87402534..87402534hg38UCSC Ensembl
chr9:90017449..90017449hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17162528
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5640702
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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