A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5584438



Internal ID21532978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:3116966..3117034hg38UCSC Ensembl
chr3:3158650..3158718hg19UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17130605
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5584438
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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