A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5609732



Internal ID21558037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:134113561..134113561hg38UCSC Ensembl
chr3:133832405..133832405hg19UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17120311
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5609732
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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