A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16935361



Internal ID24291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:109261602..109261746hg38UCSC Ensembl
chr3:108980449..108980593hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg38145
hg19145
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5437366
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16935361
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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