A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5609773



Internal ID21558078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:11750..11750hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38157
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17139198, nssv17130359, nssv17136289
SamplesNA19239, NA12878, HG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5609773
Frequency
Sample Size35
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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