A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5999945



Internal ID21909288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:474737..474810hg38UCSC Ensembl
chr5:474852..474925hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17557339
Samples
Known GenesSLC9A3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5999945
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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