A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5569097



Internal ID21517450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:38326852..38326918hg38UCSC Ensembl
chr3:38368343..38368409hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17133173
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5569097
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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