A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5584496



Internal ID21533037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:194382030..194382131hg38UCSC Ensembl
chr3:194102759..194102860hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17125588
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5584496
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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