A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16904338



Internal ID3715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:5346435..5348771hg38UCSC Ensembl
chr1:5406495..5408831hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg382337
hg192337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5419140
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16904338
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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