A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17533898



Internal ID21858254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4081931..4100069hg38UCSC Ensembl
chr3:4123615..4141753hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3818139
hg1918139
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5993372
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17533898
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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