A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17555940



Internal ID21880295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:12878464..12881759hg38UCSC Ensembl
chr3:12919963..12923258hg19UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg383296
hg193296
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5991124
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17555940
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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