A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17540748



Internal ID21865103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141665719..141665913hg38UCSC Ensembl
chr3:141384561..141384755hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38195
hg19195
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5992034
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17540748
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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