A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16929280



Internal ID20233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4041979..4088941hg38UCSC Ensembl
chr3:4083663..4130625hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3846963
hg1946963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5437680
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16929280
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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