A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5566609



Internal ID21514937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:102564930..102565267hg38UCSC Ensembl
chr3:102283774..102284111hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17126320
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5566609
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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