A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16942790



Internal ID29197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:193041144..193041218hg38UCSC Ensembl
chr3:192758933..192759007hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5442051
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16942790
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.007493


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