A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16944237



Internal ID30159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:195065172..195066723hg38UCSC Ensembl
chr3:194785901..194787452hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg381552
hg191552
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6140130
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16944237
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.265224


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