A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16930232



Internal ID20897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:20973162..20977236hg38UCSC Ensembl
chr3:21014654..21018728hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg384075
hg194075
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5444833
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16930232
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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