A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17543266



Internal ID21867621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:32841048..32841100hg38UCSC Ensembl
chr5:32841154..32841206hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5999626
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17543266
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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