A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17541297



Internal ID21865652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:32448962..32451039hg38UCSC Ensembl
chr5:32449068..32451145hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg382078
hg192078
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5999398
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17541297
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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