A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981944



Internal ID21891287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:171096451..171096528hg38UCSC Ensembl
chr1:171065592..171065669hg19UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17527429
Samples
Known GenesFMO3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981944
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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