A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16955911



Internal ID37916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:133509793..133535700hg38UCSC Ensembl
chr4:134430948..134456855hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3825908
hg1925908
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5454891
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16955911
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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