A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5581432



Internal ID21529931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:146709690..146710495hg38UCSC Ensembl
chr3:146427477..146428282hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38806
hg19806
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17135557
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5581432
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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