A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5879399



Internal ID22654368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151559896..151560032hg38UCSC Ensembl
chr1:151532372..151532508hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17365506
Samples
Known GenesTUFT1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5879399
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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