A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16940990



Internal ID28031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:139167574..139172800hg38UCSC Ensembl
chr3:138886416..138891642hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg385227
hg195227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5441890
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16940990
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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