A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17537623



Internal ID21861978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:170408935..170409011hg38UCSC Ensembl
chr3:170126723..170126799hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5992119
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17537623
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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