A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17542767



Internal ID21867122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:53410833..53419269hg38UCSC Ensembl
chr3:53444860..53453296hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg388437
hg198437
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5994142
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17542767
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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