A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17543589



Internal ID21867944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:109324168..109324263hg38UCSC Ensembl
chr3:109043015..109043110hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5991431
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17543589
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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