A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16930327



Internal ID20961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:24704041..24779037hg38UCSC Ensembl
chr3:24745532..24820528hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg3874997
hg1974997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5435832
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16930327
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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