A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17544650



Internal ID21869005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:88016293..88016957hg38UCSC Ensembl
chr3:88065443..88066107hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg38665
hg19665
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5994353
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17544650
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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