A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5415884



Internal ID195131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151554445..151556447hg38UCSC Ensembl
chr1:151526921..151528923hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg382003
hg192003
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16890304
Samples
Known GenesTUFT1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5415884
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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