A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17544849



Internal ID21869204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:176419760..176419839hg38UCSC Ensembl
chr3:176137548..176137627hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5991926
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17544849
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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