A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17550502



Internal ID21874857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:46180622..46180751hg38UCSC Ensembl
chr3:46222114..46222243hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5993867
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17550502
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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