A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17417254



Internal ID22475124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:43861465..43861713hg38UCSC Ensembl
chr3:43902957..43903205hg19UCSC Ensembl
Cytoband3p21.33
Allele length
AssemblyAllele length
hg38249
hg19249
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5904723
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17417254
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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