A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16940039



Internal ID27412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:153881419..153896197hg38UCSC Ensembl
chr3:153599208..153613986hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3814779
hg1914779
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5442776
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16940039
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.002342


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