A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981511



Internal ID21890854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151847240..151847292hg38UCSC Ensembl
chr1:151819716..151819768hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17522456
Samples
Known GenesTHEM5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981511
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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