A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16892111



Internal ID168931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:168196398..168196458hg38UCSC Ensembl
chr1:168165636..168165696hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5427071
Supporting Variants
Samples
Known GenesTIPRL
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16892111
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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