A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16944415



Internal ID30282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:190361924..190369891hg38UCSC Ensembl
chr3:190079713..190087680hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg387968
hg197968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5450005
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16944415
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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