A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17547473



Internal ID21871828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:107406259..107406351hg38UCSC Ensembl
chr3:107125106..107125198hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5990953
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17547473
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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