A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5583834



Internal ID21532364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:143889674..143889855hg38UCSC Ensembl
chr3:143608516..143608697hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38182
hg19182
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17122654
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5583834
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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