A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16890449



Internal ID167798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:158485382..158544049hg38UCSC Ensembl
chr1:158455172..158513839hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg3858668
hg1958668
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5432731
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16890449
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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