A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6057060



Internal ID21966293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:179850801..179850801hg38UCSC Ensembl
chr1:179819936..179819936hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17535250
Samples
Known GenesTOR1AIP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6057060
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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