A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16894206



Internal ID170294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:12192097..12205344hg38UCSC Ensembl
chr1:12252154..12265401hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3813248
hg1913248
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5431646
Supporting Variants
Samples
Known GenesTNFRSF1B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16894206
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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