A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5643771



Internal ID21592076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:121961698..121961698hg38UCSC Ensembl
chr5:121297393..121297393hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17133349
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5643771
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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