A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5991111



Internal ID21900454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:126074885..126075021hg38UCSC Ensembl
chr3:125793728..125793864hg19UCSC Ensembl
Cytoband3q21.2
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17554079
Samples
Known GenesSLC41A3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5991111
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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