A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16890858



Internal ID168079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155304397..155304471hg38UCSC Ensembl
chr1:155274188..155274262hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5418947
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16890858
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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