A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16891596



Internal ID168589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:167056767..167057240hg38UCSC Ensembl
chr1:167026004..167026477hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg38474
hg19474
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5418445
Supporting Variants
Samples
Known GenesGPA33
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16891596
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.017182


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