A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5582324



Internal ID21530835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:34093225..34098990hg38UCSC Ensembl
chr3:34134717..34140482hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg385766
hg195766
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17125828
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5582324
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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